EP1331999A2 - Dispositifs et procedes de multiplexage de puces a adn - Google Patents
Dispositifs et procedes de multiplexage de puces a adnInfo
- Publication number
- EP1331999A2 EP1331999A2 EP01987105A EP01987105A EP1331999A2 EP 1331999 A2 EP1331999 A2 EP 1331999A2 EP 01987105 A EP01987105 A EP 01987105A EP 01987105 A EP01987105 A EP 01987105A EP 1331999 A2 EP1331999 A2 EP 1331999A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- preferred
- nucleic acid
- cartridge
- electrode
- etms
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L9/00—Supporting devices; Holding devices
- B01L9/52—Supports specially adapted for flat sample carriers, e.g. for plates, slides, chips
- B01L9/527—Supports specially adapted for flat sample carriers, e.g. for plates, slides, chips for microfluidic devices, e.g. used for lab-on-a-chip
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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- G—PHYSICS
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/5308—Immunoassay; Biospecific binding assay; Materials therefor for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites
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- G—PHYSICS
- G01—MEASURING; TESTING
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54366—Apparatus specially adapted for solid-phase testing
- G01N33/54373—Apparatus specially adapted for solid-phase testing involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
- G01N33/5438—Electrodes
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- G—PHYSICS
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- G01N35/00584—Control arrangements for automatic analysers
- G01N35/00722—Communications; Identification
- G01N35/00871—Communications between instruments or with remote terminals
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- B01L2300/0627—Sensor or part of a sensor is integrated
- B01L2300/0636—Integrated biosensor, microarrays
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- B01L2300/0627—Sensor or part of a sensor is integrated
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- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
- B01L2300/0819—Microarrays; Biochips
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
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- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
- B01L2300/0877—Flow chambers
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- B01L2300/18—Means for temperature control
- B01L2300/1805—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
- B01L2300/1822—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using Peltier elements
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01L2300/00—Additional constructional details
- B01L2300/18—Means for temperature control
- B01L2300/1805—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
- B01L2300/1827—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using resistive heater
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0475—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
- B01L2400/0487—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure fluid pressure, pneumatics
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/06—Valves, specific forms thereof
- B01L2400/0605—Valves, specific forms thereof check valves
- B01L2400/0611—Valves, specific forms thereof check valves duck bill valves
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/06—Valves, specific forms thereof
- B01L2400/0633—Valves, specific forms thereof with moving parts
- B01L2400/0638—Valves, specific forms thereof with moving parts membrane valves, flap valves
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/06—Valves, specific forms thereof
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- B01L2400/0655—Valves, specific forms thereof with moving parts pinch valves
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/06—Valves, specific forms thereof
- B01L2400/0633—Valves, specific forms thereof with moving parts
- B01L2400/0661—Valves, specific forms thereof with moving parts shape memory polymer valves
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L7/00—Heating or cooling apparatus; Heat insulating devices
- B01L7/52—Heating or cooling apparatus; Heat insulating devices with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples
- B01L7/525—Heating or cooling apparatus; Heat insulating devices with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples with physical movement of samples between temperature zones
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y15/00—Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
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- G—PHYSICS
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/02—Devices for withdrawing samples
- G01N2001/021—Correlating sampling sites with geographical information, e.g. GPS
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/00029—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor provided with flat sample substrates, e.g. slides
- G01N2035/00099—Characterised by type of test elements
- G01N2035/00158—Elements containing microarrays, i.e. "biochip"
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- G—PHYSICS
- G01—MEASURING; TESTING
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- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N2035/00178—Special arrangements of analysers
- G01N2035/00326—Analysers with modular structure
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/11—Automated chemical analysis
Definitions
- the invention is directed to devices that allow for simultaneous multiple biochip analysis.
- the devices are configured to hold multiple cartridges comprising biochips comprising arrays such as nucleic acid arrays, and allow for high throughput analysis of samples.
- biosensors rely on electronic signals for detection.
- biosensors At least two types of biosensors are known; enzyme-based or metabolic biosensors and binding or bioaffinity sensors. See for example U.S. Patent No. 4,713,347; 5,192,507; 4,920,047; 3,873,267; and references disclosed therein. While some of these known sensors use alternating current (AC) techniques, these techniques are generally limited to the detection of differences in bulk (or dielectric) impedance.
- AC alternating current
- nucleic acid biochips based on fluorescent detection; see for example materials developed by Affymetrix (including, but not limited to, 5,800,992, 5,445,934, 5,744,305, and related patents and materials), Nanogen (including, but not limited to, 5,532,129, 5,605,662, 5,565,322 and 5,632,957 and related patents and materials), Southern (EP 0 373 023 B1) and Synteni/lncyte (WO 95/35505 and related patents and materials).
- electronic detection of nucleic acids using electrodes is also known; see for example U.S. Patent Nos.
- the present invention provides biochip cartridges comprising one or more reaction chambers, such as a nucleic acid amplification chamber.
- the chambers are configured to include inlet and outlet ports, valves to control the movement of fluid into and out of the chamber and pumps.
- the biochip cartridge comprises a detection chamber with an array of electrodes.
- the biochip cartridge comprises one or more thermal heaters.
- Figures 1 A-1 J depict a number of different detection chamber embodiments.
- Figures 1 A-1 F depict alternative detection chamber geometries in which the inlet port 100 is positioned at the top of the chamber.
- the outlet port 101 can have several configurations.
- the outlet port is located at the top of the chamber but does not vent to the outside.
- the outlet port 101 is positioned at the top and vents outside.
- the outlet port 101 is located to the side of the chamber.
- the outlet port 101 comes off of the inlet port 100.
- the electrode array 103 is positioned within a reaction chamber 102, which may be formed from a gasket, a recess in the underlying printed circuit board or from the housing 104.
- the reaction chamber is shaped like an inclined diamond; in Figure 1B, the reaction chamber is shaped like a diamond; in Figure 1D, the reaction chamber is circular in shape; in Figure 1 E, the reaction chamber is triangular in shape; and, in Figure 1 F, the reaction chamber is shaped like a square.
- Figure 1 F depicts an embodiment in which reference electrodes 106 are located in the inlet and/or the outlet channels.
- the reference electrodes are preferably AgCI.
- the reference electrodes may be coated with AgCI before placing in the cartridge.
- FIG. 1G depicts a biochip 105 comprising a reaction chamber 102 with an electrode array 103, a PCR chamber 115, a buffer chamber 170, an air pimp chamber or other mechanism for moving fluid 116, one or more valves for controlling the movement of fluid 171 , temperature sensors 172, heating elements integrated into the device 173, a mixing element 174, reference electrodes 106, inlet 100 and outlet 101 ports, a microchannel 110, a silicon gasket 104B with a cutout for the detection chamber 113 and a cap 130.
- Figure 1 H depicts the top surface of an electronic biochip.
- the electrode array 103 is configured such that each electrode is connected via a wire lead 109 to a contact pad or interconnect
- FIG. 11 and 1 J show a biochip 105 with connects that transverse the board making contact with a pogo pin connector 176.
- the connector has an array of compliant pins 177, a circuit board housing 177, and potentially an electronic multiplexer 178.
- the pin grid connector ultimately plugs into an instrument through some interface like an edge card connector via metal fingers 179. In order to ensure a good connection between the pogo pin connectors and the chip, it is common to use some type of fastener.
- Figure 2 depicts the various components that can comprise a cartridge.
- the detection chamber 102 contains an electrode array 103 connected via wires
- FIG. 2B depicts a rubber gasket 104 with a cut out for the detection chamber 113 and registration holes 112 for attaching the gasket to the biochip depicted in Figure 2A.
- Figure 2C depicts a housing 114, which can be made from plastic and is attached to the biochip via registration holes 112.
- the cartridge 114 may optionally contain a cutout 113A for the detection chamber 103 and a recessed microchannel 110 running from the inlet port 100 to the detection chamber 103.
- Figures 3A and 3B depict two views, top view ( Figure 3A) and an angled front view (Figure 3B) of the cartridge holders 129 used to hold the cartridges during sample loading.
- the cartridge holder 129 can hold several cartridges 114 with attached biochips 105.
- a cartridge cap 130 which can be taken on and off via a "snap-in lock”.
- Figures 3C and 3D depict different views of a cartridge with a cap.
- the cap 130 is configured to include a snap-in lock 132, that locks into a slot 133 in the cartridge 114.
- the cap has been configured to include a seal 134 for the sample introduction module 136.
- the seal 134 comprises a plastic plug surrounded by cellulose or another hydrophobic material that allows air to pass but not liquid.
- the cartridge 114 has been configured to include sample introduction module 136, and a PCR chamber 115.
- the cartridge 114 is attached to a biochip comprising a reaction chamber 102, an electrode array 103, connected via wires 109 to interconnects 108, a microchannel 110, and an outlet port 101.
- Figure 3D illustrates a side vies of the cap 130, the cartridge 114 configured to contain a PCR chamber 115, and a chip 105.
- Figure 3E depicts a side view of several cartridge assemblies lined up as they would appear in the cartridge holder.
- the cap 130 is attached to the cartridge 114, which has been configured to comprise a sample introduction module 136 and a PCR chamber 115. Attached to the cartridge is a biochip 105.
- Figures 4A and 4B depict different views of a multiplexing device 137.
- a side and top view of the multiplexing device 137 illustrates the cartridge/station pairs 139 and a drawer 138.
- the multiplexing device 137 is illustrated with the stations 141 for holding the cartridges and an open drawer 138.
- Figure 5 illustrates a schematic of an electronic circuit designed to monitor the sample temperature with a thermal sensor inside the cartridge.
- This version of the design uses a resistive temperature device composed of a copper trace.
- the circuitry can be used in feedback system for thermal control of the cartridge temperature.
- FIG. 6 illustrates the thermal control logic.
- This feedback mechanism employs a Proportional Integral Derivative (PID) algorithm.
- PID Proportional Integral Derivative
- FIG 7 illustrates the layout of a multiplexing device.
- the device has eight independent modules.
- each module has six card-edge connectors 141 and a signal processing printed circuit board 140.
- the power supply 145 Directly underneath the modules is the power supply 145.
- Adjacent to the power supply is a bus bar 150 for power distribution.
- Figure 7 depicts the stations into which the cartridges are inserted.
- a cartridge 114 with a cap 130 is shown inserted into an card edge connector 141.
- Figure 8 is a block diagram for the software application used to control the multiplexing device.
- Figures 9A-F depict a variety of different valves that may be used in the present invention.
- Figure 9A depicts a duck bill valve 144 within a microchannel 110 that can be used to control the flow of liquid in one direction, but not the other.
- Figure 9B depicts a cantilever valve 146. In this embodiment, voltage, applied via electrodes 147 is used to open and close the cantilever valve 146.
- Figure 9C depicts a plunger type valve mechanism. In this embodiment, a plunger valve 148 can be opened and closed via the use of a shape memory wire 149.
- Figures 9D and 9E depict rotary valves. In the embodiment shown in Figure 9D, an external force must be applied to rotate the rotary valve 151.
- a shape memory wire 149 is used to rotate the rotary valve 151.
- Figure 9F depicts a thermally actuated valve that comprises a portion of the microchannel 110 with a flexible membrane 152 that can be filled with liquid or air 153 for use in conjunction with a heater 154.
- Figure 9G depicts a generic pump design in which a chamber 156 through which air and/or liquid can flow is attached to an inlet port 100 with a valve, such as a cantilever valve 146, to control movement into the chamber and an outlet port 101 with a valve 146A, to control movement out of the chamber.
- An external device 181 such as a PZT, can be used to compress chamber 156.
- a heater 182 can be actuated expanding the volume of the gas or liquid in chamber 156.
- FIG 10A is a side view of a biochip 105 depicting an embodiment in which a thermal heater is incorporated into the chip.
- the resistive heaters 157 are overlaid with a layer of copper 158.
- the copper layer is overlaid with printed circuit board 125, which is covered with solder mask 159.
- Figures 10B illustrates one means of creating thermal zones in a biochip 105.
- successive thermal zones 161, 162, 163 comprising several rows of resistive heaters 157 are overlaid with a serpentine microchannel 164.
- Discrete temperature zones are maintained by controlling the minimum separation distance between resistive heater 161, 162, and 163 as well as varying the thermal properties of the separating materials, the device illustrated in Figure 10B can be used in conjunction with a pumping device to transport a fluid between temperature zones and perform biological reactions that require heat cycling like PCR.
- Figure 10C depicts a biochip analogous to Figure 10B, but made out of ceramic 165 with imbedded heaters 166 and corresponding edge connections 108. The temperature difference between the thermal zones is maintained by creating air pocket cut-outs 167 that have a lower thermally conductivity than the surrounding ceramic.
- Figure 11 depicts a bar code reader 142 reading a bar code 143.
- Figures 12 describes a bar code usage scenario.
- Figure 13 highlights the benefits of using a bar code in combination with the devices of the present invention.
- FIGs 14 A and B depict a preferred embodiment of a biochip 105 with registration holes 112 for the attachment of a cartridge 114.
- the top surface of a biochip 105 is depicted showing the registration holes 112, an electrode array 103 and interconnects 108.
- a cartridge 114 is shown overlaying the biochip 105 illustrated in Figure 14A.
- the cartridge 114 includes registration pins 107 for attaching the cartridge to the biochip.
- the registration pins are plastic.
- the cap gasket 134 is depicted as an insert within the sample introduction chamber 136.
- Figure 15A depicts sample loading using a pipet tip 144 into a cartridge 114 inserted into a station 141 of a multiplexing device 137.
- FIGs 15B and C depict an alternative embodiment for attaching a cartridge to a biochip.
- the biochip 105 is designed to have alignment slots 118.
- the cartridge is configured to have registration pins 107 that fit into the registration holes on the sides of the biochip.
- Also depicted in Figure 15C is the use of a pipet tip 144 for loading a sample into a sample introduction chamber 136.
- Figure 16 depicts a sine wave and its corresponding vector notation.
- Figure 17 depicts the visualization of the sine wave shown in Figure 16 using vector notation.
- the two values can be R and ⁇ , but as shown in the Figure 17 they can also be an (XN) pair separated by one quarter of an oscillation, i.e. by 90°.
- Figures 18 and 19 are examples of R and ⁇ traces for the fourth harmonic ACE voltammetry.
- Figures 20 and 21 depict that the R space signal distorts as the signal shrinks relative to the size of the background.
- Figures 22 through 25 illustrate how the use of cartesian coordinates simplifies the dependence of of
- Figure 26 depicts an AC voltage-4 trace that has a large signal relative to the background.
- Figure 26 is obtained If, in a two-dimensional graph, the tip of the data vector as a function of voltage (one point is plotted every 10 mV) is plotted.
- Figures 27and 28 depict the result when a frame of reference is chosen such that the X and Y axes straddles the signal, ln this case, the signal contributes strongly to both X and Y.
- Figures 29 and 30 depicts the signal that is observed when an axis pair that is roughly parallel and perpendicular to the signal (rotated 45° with respect to the axes drawn in Figure 26) is chosen. In this case, very little of the signal contributes to the perpendicular vector.
- Figures 31 through 35 illustrate the vectoral sum method.
- a new pair of axes need to be chosen to straddle any existing electrochemical signal.
- a way is needed to measure the signal's direction.
- One such way is using a vectoral sum.
- Figure 31 Let the grouping of three points shown in Figure 31. If we consider these points as vectors, we can add them by summing their coordinates. This summation of the vectors provides a reasonable angle for the best line through the data that passes through (0,0). This angle is called the "optimal phase.”
- the summation is drawn in Figure 32.
- Figure 33 shows how the three sample data points cluster around the line.
- An advantage to this method is that the results are weighted by the length of the vectors of the original data points. For example, if we add a small data point to the sample grouping, the results are shown in Figure 34 and 35.
- Figures 36 through 41 illustrate the complications that must be considered when using the vectoral sum to calculate the optimal phase for fitting a signal. For example, if the electrochemical signal is shaped such that portions of it cancel each other out when completing the calculation described above, the first one half of the data must be rotated 180°. Taking the data shown in Figure 26, we calculate the optimal phase using the data as shown in Figure 36. The resulting line is overlaid on the original data, at Figure 37. The angle of the line drawn in Figures 36 and 37 (101°) is what was used to choose the X and Y axes (at ⁇ 45°) for this file. However, if the signal is oriented differently relative to the dividing line between rotated and unrotated segments, the stated manipulation may not yield the proper angle.
- Figures 42 through 46 illustrates the results obtained if the rapid calculations necessary to fit polynomials to the entire scan (one each along the 0 and 90° axes) are performed.
- the background is approximated as shown in Figure 42 and 43.
- the approximation to the background can be subtracted, converting the scan into something that is much more purely signal, as shown in Figure 44 and 45.
- Figure 46 depicts this as a two dimensional plot, from which an optimal phase of approximately 70° can be calculated.
- Figures 47 through 52 illustrate how behaviors not modeled are detected. To reduce total processing time, the first thing to do is to check if a scan has any gross deviations from the model that would make fitting it meaningless.
- One such feature encountered in AC voltammetry (fourth harmonic) has been the sharp peak caused by the stripping of a metallic contaminant.
- Figure 47 shows an example of one displayed in R-space. In X and Y (at ⁇ 45° from the optimal phase), the sharp spike feature remains clear, as shown in Figure 48 and 49.
- the symmetry of this feature distinguishes it from our normal signal.
- One method of monitoring this symmetry is to separate out an approximate background and compare the distribution of points above the baseline with the distribution below. For example, if we subtract a polynomial from the Y trace above, we get the results shown in Figures 50 and 51. If we now examine the distribution of data above and below the approximated background, the presence of the spike causes a larger range of values to exist below the background line than above it, as shown in Figure 52.
- Figures 53 through 58 illustrate the initial guess process required as a starting point for iterative fitting procedures.
- the known AC voltage-4 symmetry is used combined with knowledge of the characteristic width. Since the average separation between the two larger center lobes is known, the signal and shift are duplicated, the two copies in opposite directions for half of that separation. Subtracting one from the other, the center lobes interfere constructively. The absolute value of this resulting wave provides a good estimation of the height and position of the signal.
- This process is shown in Figures 53, 54 and 55 for a signal 11.9 tall at a position of 0.20 with a center lobe separation of 0.072.
- the trace in Figure 55 has its largest value, 23.25, at a position of 0.20. The position matches well with the true data value. (Both are 0.20.)
- Figure 56 the same signal is considered, but this time with an unusual peak off to one side that's slightly taller than the signal itself. In a simple maxima/minima search, this would be likely to interfere with the initial guess. However, using the initial guess, the signal remains 11.6 tall at a position of 0.20, as shown in Figure 57.
- Figure 58 is the overlay of a real data trace and the corresponding initial guess.
- Figure 62 depicts the results when the fit is not reliable because the difference between the fit and date is too large.
- Figures 63 through 65 depict the results obtained using procedures to refit scans having no observable signals.
- Figures 66 and 67 depict the results obtained using the procedures described herein.
- Figure 66 depicts the original data.
- Figure 67 depicts the data with the background subtracted.
- Figure 68 depicts the effect of various plasma treatments on the surface density of SAMs comprising capture probes.
- Figure 69 depicts the spectra of contaminants on a gold surface after various plasma treatment procedures. The major contaminant peaks of carbon and oxygen are marked out with gold peaks for the oxygen plasma treatment alone, or for the oxygen plasma followed by hydrogen plasma treatment.
- Figure 70A-F depict the effect of different mixing techniques on hybridization kinetics in an eSensorTM chamber.
- Figure 70A depicts effect of chip orientation (i.e., diffusion based kinetics) on hybridization kinetics and increased volume/z-dimension. Increased volume was obtained by increasing the thickness of the chamber using one (single tape), two (double tape) or three (triple tape) layers of tape. Chips were incubated either horizontally (H) or vertically (V).
- Figure 70B compares diffusion based kinetics using chips oriented either vertically (vdiff) or horizontally (hdiff) to mixing using a recirculation pump (vpump).
- Figure 70C compares diffusion based kinetics/vertical orientation (vdiff) to bubble assisted PZT mixing using either a square wave (vpztsquare) or a sine wave excitation (vpztsine) waveform.
- Figure 70D compares diffusion based kinetics/vertical orientation (vdiff) to thermal gradient based mixing (TG).
- Figure 70E compares diffusion based kinetics/vertical orientation to diffusion based kinetics in a biochannel/vertical orientation to diffusion based kinetics in a biochannel/horizontal orientation to bubble mixing in a biochannel/horizontal orientation.
- Figure 70F depicts acoustic based mixing (treat-H) to diffusion based kinetics using either vertical (ctrl-V) or horizontal (ctrl-H) chip orientation.
- a digital to analog converter receives a digital signal from a signal source (such as signal generating circuitry on the signal processing printed circuit board or received from a connected personal computer) and converts that signal into an analog signal which is received by filter.
- the characteristics of filter may be modified to provide frequency low-pass, high-pass, or single or multiple band-pass characteristics according to tailored the signal applied to the electrodes of the E-Chem Cell.
- the filtered signal is passed through resistor R9 (110 Kohm) before passing through a first auxiliary amplifier (AUX AMP).
- AUX AMP first auxiliary amplifier
- the signal is desirably multiplexed through multiplexer (MUX) and distributed to a plurality of auxiliary electrodes on the E-Chem cell cartridge.
- a set of reference electrodes is also disposed within the E-Chem Cell cartridge, the outputs of which are coupled to through a second multiplexer (MUX) and reference amplifier (REF AMP) and resistor R13 (110 Kohm) back to the input of first auxiliary amplifier.
- MUX second multiplexer
- REF AMP reference amplifier
- resistor R13 110 Kohm
- a set of active electrodes (36 active electrodes in this embodiment) are coupled via printed circuit board traces to a third mutiplexer.
- the output of this active electrode multiplexer is amplified by an input signal amplifier (INPUT AMP), and after further optional signal conditioning (such as filtering, gain control and/or selection) is processed through a buffer amplifier (BUFFER AMP) and converted from analog to digital (ADC) form, so that it may be communicated, processed, analyzed, stored or the like in digital form.
- INPUT AMP input signal amplifier
- BUFFER AMP buffer amplifier
- ADC analog to digital
- FIG. 72 there is illustrated an embodiment of a Thermal Control Block Diagram.
- a microprocessor communicates with an external signal source or sink via a serial communication channel or link.
- microprocessor generates a control signal to provide an indication of an ON, OFF, or FLASH status to an LED logic circuit which is coupled with and causes LED Drivers to send signals to each of six slots causing each of the slots red or green lights to be on, off, or flash.
- Microprocessor also generates a signal to DAC. This signal is amplified to power a heat sink blower to control the temperature of the heat sink.
- a heat sink temperature sensor is associated with the heat sink and this sensor generates a temperature signal which is fed back to the microprocessor in feedback manner to control operation or non-operation of the heat sink blower motor.
- the microprocessor also generates a plurality of signals which are received by a plurality of DAC and driver amplifiers to a Peltier thermal block for each slot.
- a temperature sensor is also associated with each Peltier thermal block to provide a sensed temperature indication back to the microprocessor for controlling the Peltier thermal block drive signal in feedback manner.
- Each board includes an edge connector for coupling with a communication bus, motherboard, or other interconnect as are known in the art.
- Each board in this particular embodiment further includes pad selector circuitry, memory, a CPU/lock-in amplifier, buffers, serial communication circuitry, waveform signal generators, analog-to-digital converter (ADC), filters or filter circuits, master gain circuit, current- to-voltage converter, power regulators, and chip selector (ref/mux).
- ADC analog-to-digital converter
- filters or filter circuits master gain circuit
- current- to-voltage converter current- to-voltage converter
- power regulators power regulators
- chip selector chip selector
- the present invention is directed to devices designed to receive and analyze a plurality of biochips, each comprising an array of biological moieties, such as nucleic acids or proteins, to allow high throughput analysis and detection of target analytes in samples.
- a number of samples can be simultaneously analyzed, or multiple assays can be run on a single sample.
- the devices comprise a number of cartridge stations that are configured to receive the biochips, with different types of biochips allowing different types of components.
- the stations can include a wide variety of different components, including thermocontrollers, signaling systems, sensors for leak detection, alphanumeric displays, and detectors.
- Preferred embodiments include the use of biochips comprising electrodes that rely on electrochemical detection, and thus the devices and/or stations can comprise device boards and processors.
- the biochip cartridges include substrates comprising the arrays of biomolecules, and can be configured in a variety of ways.
- the chips can include reaction chambers with inlet and outlet ports for the introduction and removal of reagents.
- the cartridges can include caps or lids that have microfluidic components, such that the sample can be introduced, reagents added, reactions done, and then the sample is added to the reaction chamber comprising the array for detection.
- the present invention provides compositions and methods for detecting the presence or absence of target analytes in samples.
- the sample solution may comprise any number of things, including, but not limited to, bodily fluids (including, but not limited to, blood, urine, serum, lymph, saliva, anal and vaginal secretions, perspiration and semen, of virtually any organism, with mammalian samples being preferred and human samples being particularly preferred); environmental samples (including, but not limited to, air, agricultural, water and soil samples); biological warfare agent samples; research samples (i.e.
- the sample may be the products of an amplification reaction, including both target and signal amplification as is generally described in PCT/US99/01705, such as PCR amplification reaction); purified samples, such as purified genomic DNA, RNA, proteins, etc.; raw samples (bacteria, virus, genomic DNA, etc.); as will be appreciated by those in the art, virtually any experimental manipulation may have been done on the sample.
- an amplification reaction including both target and signal amplification as is generally described in PCT/US99/01705, such as PCR amplification reaction
- purified samples such as purified genomic DNA, RNA, proteins, etc.
- raw samples bacteria, virus, genomic DNA, etc.
- target analyte or “analyte” or grammatical equivalents herein is meant any molecule or compound to be detected and that can bind to a binding species, defined below.
- Suitable analytes include, but are not limited to, small chemical molecules such as environmental or clinical chemical or pollutant or biomolecule, including, but not limited to, pesticides, insecticides, toxins, therapeutic and abused drugs, hormones, antibiotics, antibodies, organic materials, etc.
- Suitable biomolecules include, but are not limited to, proteins (including enzymes, immunoglobulins and glycoproteins), nucleic acids, lipids, lectins, carbohydrates, hormones, whole cells (including procaryotic (such as pathogenic bacteria) and eucaryotic cells, including mammalian tumor cells), viruses, spores, etc.
- proteins including enzymes, immunoglobulins and glycoproteins
- nucleic acids including lipids, lectins, carbohydrates, hormones, whole cells (including procaryotic (such as pathogenic bacteria) and eucaryotic cells, including mammalian tumor cells), viruses, spores, etc.
- Particularly preferred analytes are proteins including enzymes; drugs, cells; antibodies; antigens; cellular membrane antigens and receptors (neural, hormonal, nutrient, and cell surface receptors) or their ligands.
- the target analyte is a protein.
- proteins or grammatical equivalents herein is meant proteins, oligopeptides and peptides, derivatives and analogs, including proteins containing non-naturally occurring amino acids and amino acid analogs, and peptidomimetic structures.
- the side chains may be in either the (R) or the (S) configuration.
- the amino acids are in the (S) or L-configuration.
- Suitable protein target analytes include, but are not limited to, (1) immunoglobulins, particularly IgEs, IgGs and IgMs, and particularly therapeutically or diagnostically relevant antibodies, including but not limited to, for example, antibodies to human albumin, apolipoproteins (including apolipoprotein E), human chorionic gonadotropin, cortisol, ⁇ -fetoprotein, thyroxin, thyroid stimulating hormone (TSH), antithrombin, antibodies to pharmaceuticals (including antieptileptic drugs (phenytoin, primidone, carbariezepin, ethosuximide, valproic acid, and phenobarbitol), cardioactive drugs (digoxin, lidocaine, procainamide, and disopyramide), bronchodilators ( theophylline), antibiotics (chloramphenicol, sulfonamides), antidepressants, immunosuppresants, abused drugs (amphetamine, methamphetamine, canna
- any target analyte for which a binding ligand, described below, may be made may be detected using the methods of the invention.
- the target analytes are nucleic acids.
- nucleic acid or “oligonucleotide” or grammatical equivalents herein means at least two nucleotides covalently linked together.
- a nucleic acid of the present invention will generally contain phosphodiester bonds, although in some cases, as outlined below, nucleic acid analogs are included that may have alternate backbones, comprising, for example, phosphoramide (Beaucage et al., Tetrahedron 49(10):1925 (1993) and references therein; Letsinger, J. Org. Chem. 35:3800 (1970); Sblul et al., Eur. J. Biochem.
- nucleic acid analogs may find use in the present invention, ln addition, mixtures of naturally occurring nucleic acids and analogs can be made; for example, at the site of conductive oligomer or ETM attachment, an analog structure may be used. Alternatively, mixtures of different nucleic acid analogs, and mixtures of naturally occuring nucleic acids and analogs may be made.
- PNA peptide nucleic acids
- These backbones are substantially non-ionic under neutral conditions, in contrast to the highly charged phosphodiester backbone of naturally occurring nucleic acids. This results in two advantages.
- the PNA backbone exhibits improved hybridization kinetics. PNAs have larger changes in the melting temperature (Tm) for mismatched versus perfectly matched basepairs. DNA and RNA typically exhibit a 2-4°C drop in Tm for an internal mismatch. With the non-ionic PNA backbone, the drop is closer to 7-9°C. Similarly, due to their non-ionic nature, hybridization of the bases attached to these backbones is relatively insensitive to salt concentration.
- the nucleic acids may be single stranded or double stranded, as specified, or contain portions of both double stranded or single stranded sequence.
- the nucleic acid may be DNA, both genomic and cDNA, RNA or a hybrid, where the nucleic acid contains any combination of deoxyribo- and ribonucleotides, and any combination of bases, including uracil, adenine, thymine, cytosine, guanine, inosine, xathanine hypoxathanine, isocytosine, isoguanine, etc.
- nucleoside includes nucleotides as well as nucleoside and nucleotide analogs, and modified nucleosides such as amino modified nucleosides.
- nucleoside includes non-naturaily occurring analog structures. Thus for example the individual units of a peptide nucleic acid, each containing a base, are referred to herein as a nucleoside.
- the target analyte is a target sequence.
- target sequence or “target nucleic acid” or grammatical equivalents herein means a nucleic acid sequence on a single strand of nucleic acid.
- the target sequence may be a portion of a gene, a regulatory sequence, genomic DNA, cDNA, RNA including mRNA and rRNA, or others.
- the target sequence may be a target sequence from a sample, or a secondary target such as a product of an amplification reaction, etc. It may be any length, with the understanding that longer sequences are more specific.
- the complementary target sequence may take many forms.
- probes are made to hybridize to target sequences to determine the presence or absence of the target sequence in a sample.
- the target sequence may also be comprised of different target domains; for example, a first target domain of the sample target sequence may hybridize to a capture probe or a portion of capture extender probe, a second target domain may hybridize to a portion of an amplifier probe, a label probe, or a different capture or capture extender probe, etc.
- the target domains may be adjacent or separated as indicated. Unless specified, the terms “first” and “second” are not meant to confer an orientation of the sequences with respect to the 5'-3' orientation of the target sequence. For example, assuming a 5'-3' orientation of the complementary target sequence, the first target domain may be located either 5' to the second domain, or 3' to the second domain.
- Suitable target analytes include biomolecules associated with: (1) viruses, including but not limited to, orthomyxoviruses, (e.g. influenza virus), paramyxoviruses (e.g respiratory syncytial virus, mumps virus, measles virus), adenoviruses, rhinoviruses, coronaviruses, reoviruses, togaviruses (e.g. rubella virus), parvoviruses, poxviruses (e.g. variola virus, vaccinia virus), enteroviruses (e.g. poliovirus, coxsackievirus), hepatitis viruses (including A, B and C), herpesviruses (e.g.
- viruses including but not limited to, orthomyxoviruses, (e.g. influenza virus), paramyxoviruses (e.g respiratory syncytial virus, mumps virus, measles virus), adenoviruses, rhinoviruses, cor
- Vibrio e.g. V. cholerae
- Escherichia e.g. Enterotoxigenic E.
- coli Shigella, e.g. S. dysenteriae; Salmonella, e.g. S. typhi; Mycobacterium e.g. M. tuberculosis, M. leprae; Clostridium, e.g. C. botulinum, C. tetani, C. difficile, C.perfringens; Cornyebacterium, e.g. C. diphtheriae; Streptococcus, S. pyogenes, S. pneumoniae; Staphylococcus, e.g. S. aureus; Haemophilus, e.g. H. influenzae; Neisseria, e.g. N. meningitidis, N.
- gonorrhoeae Yersinia, e.g. G. lambliaY. pestis, Pseudomonas, e.g. P. aeruginosa, P. putida; Chlamydia, e.g. C. trachomatis; Bordetella, e.g. S. pertussis; Treponema, e.g. T. palladium; and the like.
- Suitable target analytes include, but are not limited to, (1) enzymes (and other proteins), including but not limited to, enzymes used as indicators of or treatment for heart disease, including creatine kinase, lactate dehydrogenase, aspartate amino transferase, troponin T, myoglobin, fibrinogen, cholesterol, triglycerides, thrombin, tissue plasminogen activator (tPA); pancreatic disease indicators including amylase, lipase, chymotrypsin and trypsin; liver function enzymes and proteins including cholinesterase, bilirubin, and alkaline phosphotase; aldolase, prostatic acid phosphatase, terminal deoxynucleotidyl transferase, and bacterial and viral enzymes such as HIV protease; (2) hormones and cytokines (many of which serve as ligands for cellular receptors) such as erythropoietin (EPO), thrombo
- Suitable target analytes include carbohydrates, including but not limited to, markers for breast cancer (CA15-3, CA 549, CA 27.29), mucin-like carcinoma associated antigen (MCA), ovarian cancer (CA125), pancreatic cancer (DE-PAN-2), prostate cancer (PSA), CEA, and colorectal and pancreatic cancer (CA 19, CA 50, CA242).
- Suitable target analytes include metal ions, particularly heavy and/or toxic metals, including but not limited to, aluminum, arsenic, cadmium, selenium, cobalt, copper, chromium, lead, silver and nickel.
- the methods of the invention are used to detect pathogens such as bacteria.
- preferred target sequences include rRNA, as is generally described in U.S. Patent Nos. 4,851,330; 5,288,611; 5,723,597; 6,641 ,632; 5,738,987; 5,830,654; 5,763,163; 5,738,989; 5,738,988; 5,723,597; 5,714,324; 5,582,975; 5,747,252; 5,567,587; 5,558,990; 5,622,827; 5,514,551; 5,501 ,951 ; 5,656,427; 5.352.579; 5,683,870; 5,374,718; 5,292,874; 5,780,219; 5,030,557; and 5,541,308, all of which are expressly incorporated by reference.
- analytes may be detected using the present methods; basically, any target analyte for which a binding ligand, described below, may be made may be detected using the methods of the invention. While many of the techniques described below exemplify nucleic acids as the target analyte, those of skill in the art will recognize that other target analytes can be detected using the same systems.
- the target analyte is prepared using known techniques.
- the sample may be treated to lyse the cells, using known lysis buffers, electroporation, etc., with purification and/or amplification as needed, as will be appreciated by those in the art.
- the target analyte is a nucleic acid
- the target sequence may be amplified as required; suitable amplification techniques are outlined in PCT US99/01705, hereby expressly incorporated by reference.
- techniques to increase the amount or rate of hybridization can also be used; see for example WO 99/67425 and U.S.S.N.s 09/440,371 and 60/171,981, all of which are hereby incorporated by reference.
- the samples comprising the target analytes can be added to cartridges comprising the biochips as is outlined in greater detail below.
- carrier herein is meant a casing or housing for the biochip.
- the cartridge can take on a number of configurations and can be made of a variety of materials. Suitable materials include, but are not limited to, fiberglass, teflon, ceramics, glass, silicon, mica, plastic (including acrylics, polystyrene and copolymers of styrene and other materials, polypropylene, polyethylene, polybutylene, polycarbonate, polyurethanes, TeflonTM, and derivatives thereof, etc.), etc. Particularly preferred cartridge materials are plastic (including polycarbonate and polyproplylene) and glass.
- the cartridge can comprise a number of components, including reaction chambers, inlet and outlet ports, heating elements including thermoelectric components, RF antennae, electromagnetic components, memory chips, sealing components such as gaskets, electronic components including interconnects, multiplexers, processors, etc.
- the cartridge comprises a reaction chamber.
- the reaction chamber comprises a space or volume that allows the contacting of the sample to the biochip array.
- the volume of the reaction chamber can vary depending on the size of the array and the assay being done. In general, reaction chamber ranges from 1 nL to about 1 mL, with from about 1 to about 250 ⁇ l being preferred and from about 10 to about 100 ⁇ l being especially preferred. In some embodiments, to avoid the introduction of air bubbles into the reaction chamber (which can be disruptive to detection), the reaction chamber is less than the size of the sample to be introduced, to allow a slight overflow and thus ensure that the reaction chamber contains little or no air.
- the biochip cartridge can be configured to include additional chambers that can used for any number of different reactions, such as sample preparation, cell lysis, rare target capture/concentration, sample clean-up, nucleic acid amplification, including PCR, post-amplification clean-up, sample concentration, reagent storage, mixing baffles/devices, etc.
- the reaction chamber may be configured for other types of reactions as generally described below.
- the biochip cartridge reaction chamber is configured to include at least one nucleic acid amplification chamber.
- multiple amplification chambers may be used. That is, a cartridge may comprise from about 1 to about 10 or more chambers, with 2, 3, 4, 5, 6, 7, 8 or 9 also being preferred.
- the biochip cartridge reaction chamber is configured to include at least one PCR chamber.
- multiple PCR chambers may be used. That is, a cartridge may comprise from about 1 to about 10 or more chambers, with 2, 3, 4, 5, 6, 7, 8 or 9 also being preferred.
- the chamber of the cartridge should be made from biocompatible materials.
- materials that provide a surface that retards the non-specific binding of biomolecules e.g. a "non sticky" surface
- a "non sticky" surface prevents enzymatic components of the reaction mixture from sticking to the surface and being unavailable in the reaction.
- the biocompatible properties of the chamber may be improved by minimizing the surface area.
- Biocompatible materials include, but are not limited to, plastic (including acrylics, polystyrene and copolymers of styrene and other materials, polypropylene, polyethylene, polybutylene, polyimide, polycarbonate, polyurethanes, TeflonTM, and derivatives thereof, etc.)
- Other configurations include combinations of plastic and printed circuit board (PCB; defined below).
- PCB printed circuit board
- at least one side of the chamber is printed circuit board, while one or more sides of the chamber are made from plastic, ln a preferred embodiment, three sides of the chamber are made from plastic and one side is made from printed circuit board.
- the chambers, channels, valves, pumps, etc. of the systems described herein may be coated with a variety of materials to reduce non-specific binding. These include proteins such as caseins and albumins (bovine serum albumin, human serum albumin, etc.), parylene, other polymers, etc.
- the reaction chamber of the cartridge comprises an inlet port for the introduction of the sample to be analyzed.
- multiple inlet ports may be used, that may feed from a variety of storage chambers or from the outside of the chamber.
- the inlet port may optionally comprise a seal to prevent or reduce the evaporation of the sample or reagents from the reaction chamber.
- the seal comprises a gasket, or valve through which a pipette or syringe can be pushed.
- the gasket or valve can be rubber or silicone or other suitable materials, such as materials containing cellulose.
- the reaction chamber can be configured in a variety of ways.
- the reaction chamber is configured to minimize the introduction or retention of air bubbles or other sample impurities.
- the inlet port allows the flow of fluid sample into the "bottom” of the reaction chamber, to allow the escape of air or fluid through the "top” of the reaction chamber, for example through an outlet port.
- the reaction chamber further comprises an outlet port to allow air or excess sample to exit the reaction chamber.
- the outlet port vents to either a waste storage well, as is further described below, to an external surface of the chip or cartridge, or, in a preferred embodiment, back into the inlet port.
- a preferred embodiment utilizes a system wherein the exit port vents to the inlet port, preferably above the point of loading.
- the tip of the pipette extends below the exit port, such that air from the exit port is not introduced into the reaction chamber.
- the materials of the cartridge housing and biochip can be chosen to be similar in hydrophobicity or hydrophilicity, to avoid the creation of air bubbles.
- reaction chamber/inlet and/or outlet ports optionally include the use of valves.
- a semi-permeable membrane or filter may be used, that preferentially allows the escape of gas but retains the sample fluid in the chamber.
- porous teflons such as GortexTM allow air but not fluids to penetrate.
- a reaction chamber in the biochip cartridge (such as a PCR chamber) has one or more valves controlling the flow of fluids into and out of the chamber.
- the number of valves in the cartridge depends on the number of channels and chambers.
- the biochip cartridge is designed to include one or more loading ports or valves that can be closed off or sealed after the sample is loaded. It is also possible to have multiple loading ports into a single chamber; for example, a first port is used to load sample and a second port is used to add reagents.
- the biochip cartridge may have a vent. The vent can be configured in a variety of ways.
- the vent can be a separate port, optionally with a valve, that leads out of the reaction chamber.
- the vent may be a loop structure that vents liquid and/or air back into the inlet port, as generally depicted in Figure 1 F.
- Valves can be multi cycle or single cycle valves. By “multicycle” valves is meant that the valve can be opened and closed more than once.
- single cycle valves or “burst valves” or “one time valves” herein is meant a valve that is closed and then opened or opened and then closed but lacks a mechanism for restoring the valve to its original position.
- Valves may also be check valves, which allow fluid flow in only one direction, or bi-directional valves.
- check valves are used to prevent fluid from going in and out of the reaction chamber during reactions.
- check valves are used when in embodiments in which it is desirable to have fluids and/or air flow in one direction, but not the other. For example, when the chamber is filled and thus compressed, air and liquid flow out. Conversely, valves can be used to empty the chamber as well.
- Types of check valves that can be used include, but are not limited to, duck bill valves (Vernay, www.vernay.com), cantilevers, bubble valves, etc.
- valve is a duck bill valve as generally depicted in Figure 9A.
- valves are “one way” valves, in that fluid can flow through in one direction but not the other.
- the valve is a cantilever valve.
- cantilever valves can also be configured for use in pumping systems as described below.
- a cantilever valve comprising a metal is used.
- the application of a voltage can either open or close a valve. See Figure 9B.
- a heat pump is incorporated into the system for opening and closing the cantilever valve.
- the check valves are made out of metals such as gold and copper such that the check valve functions as a cantilever when heat is applied.
- an actuating force is not used to pull down the valve, rather they have a restraining force that prevents them from going in the other direction.
- a thermally actuated" valve that comprises a portion of the microchannel with a flexible membrane filled with air or liquid can be used in conjunction with a heater. The application of heat causes the fluid to expand, blocking the channel. See Figure 9F.
- piezoelectric (PZT) mixers are used as valves. These can be built out of silicon (obtained from Frauhoffer), plastic (obtained from IMM) or PCB. Other materials can be used in combination with check valves include materials that can be used to block an inlet or an outlet port. Such materials include wax or other polymeric materials, such as poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymers (PEO-PPO-PEO) known commercially as Pluronics ( BASF; Pluronic F-127, Sigma) or Synperonic (ICI), that melt for use as membranes or plugs. These materials share the common feature that they can go from a solid to a liquid at a given temperature. These types of systems are used in conjunction with heaters, described below.. For example, heat is applied to melt the material, thus "opening" the valve.
- PEO-PPO-PEO poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock cop
- the burst valve is a film of metal or polymer.
- a free standing gold film is used, that is constructed using standard techniques as outlined herein, by etching away a support surface. The gold membrane dissolves upon application of a voltage and Cl" ions. See for example www.mchips.com; Santini, J.T., et al., 1999, Nature, 397:335-338; both of which are incorporated by reference in their entirety.
- a combination of check valves and wax plugs are used. In other embodiments, a combination of check valves and gold membranes are used.
- valves include mechanical means. These can frequently be bi-directional valves.
- a shape memory wire can be attached to a plunger blocking a channel. By applying a current to the wire, the wire contracts and moves the plunger out of the way, thereby opening the channel. Conversely, the plunger can be drawn into the channel to block the channel. See Figure 9C.
- Rotary valves can be configured in a variety of ways, as depicted in Figures 9D and 9E.
- an external force must be applied for rotation (i.e., a screw driver or stepper motor).
- a shape memory wire can be used, such that the application of heat or current will shrink the wire to rotate the valve. See Figure 9E.
- valves may be used in to control the flow of liquids from into and out of the various chambers of the present invention.
- examples of commercially available valves include, MEMS (micro-electro-mechanical systems) micro valves (http://www.redwoodmicro.com).
- MEMS micro-electro-mechanical systems
- TiNi liquid microvalve TiNi Alloy Company, San Leandro, CA
- TiNi pneumatic microvalves TiNi Alloy Company, San Leandro, CA
- silicon micro valves Bosch, D., et al., Sensors and Actuators A, 37-38 (1993) 684-692).
- valves and pumps include research foundations such as Chronos (http://www.memsrus.com): Institute for Microtechnology - Mainz (http://www.imm-mainz.de/); Microsystems integration group - Swiss Fed. Inst.
- either an "on chip” or “off chip” pump is used to move fluids from one area or chamber of the cartridge to another.
- a general design for a pump includes a chamber through which air and/or liquid can flow; an inlet and outlet port, and valves. Fluid is moved through the pump via the application of some force, such as heat, pressure, to the chamber.
- pumps may be designed for single use or be reusable. Generally, reusable pumps have valves, i.e., check valves, that bias the flow of fluid in one direction. Single use pumps lack valves. Thus, almost any type of pump can be built as long as a mechanism for changing the volume in the chamber and restricting back flow is included.
- the fluid or gas is displaced out of the chamber through the check valve.
- the chamber expands and draws liquid in through the pump inlet.
- a heater can be placed inside the chamber and the temperature of the gas or liquid can be raised, causing it to expand.
- the liquid is forced out of the chamber through the outlet.
- the fluid is draw in through the inlet. See Figure 9G.
- a device such as a moving piston is used to create suction, however cooling of gases, vacuum chambers and gas consuming reactions can be used.
- suction is used to move liquid in or out of the chamber, a vacuum may be created elsewhere in the system.
- an "air pump” is used to move the liquid out of the PCR chamber.
- heaters are also described below
- more than one heater is incorporated in a chip to create "heater zones”.
- Air chambers or pockets are located over the heater zones. The air chambers are connected to the reaction chamber via a channel that runs up to the top of the reaction chamber with a valve or a plug blocking it off. When the air is heated, it expands. The resulting build up in pressure forces the valve or plug to move out of the way, thereby forcing the liquid out of the chamber via an outlet port.
- a low boiling liquid in place of air.
- the low boiling liquid expands when heated and displaces the liquid contained in the reaction chamber.
- a chemical reaction may be used to move liquid out of the reaction chamber.
- the chemical reaction used to expand car air bags may be used to move liquid out of the reaction chamber, or other reactions in which gases are generated.
- TiNi alloys, nitinol wire, or “shape memory metals” can be used to mechanically actuate a syringe driven pump.
- TiNi alloys, nitinol wire or “shape memory metals” herein is meant materials that when heated above a certain transition temperature contract (i.e., usually up to 3 to 5% over the original length of the metal), thereby changing shape.
- Other materials that change shape upon heating include shape memory plastics.
- a spring that can be released is compressed or restrained within the body of the cartridge.
- wax may be used to hold a spring in its compressed state. Upon heating, the wax is melted, and the spring is released, thereby generating sufficient force to move a piston and displace liquid.
- Other versions include incorporating materials that change from solids to liquids at a given transition temperature, or moving a mechanical blockade from the spring's pathway.
- PZT PZT driven actuations
- a material comprised of lead, zirconium and titanium which upon application of a voltage undergoes a rearrangement of the crystal lattice and generates a force and a displacement. This so called piezoelectric effect can be used to constrict and expand a pump chamber and result in a net movement of liquid.
- Other materials like shape memory alloys that under a change in shape upon application of a current such that the temperature of the metal is raised above a certain transition temperature can also be used.
- commercially available micro pumps may be used in to move liquid from one location to another in the cartridge.
- Examples of commercially available pumps include, moulded plastic micro pumps available from IMM (see [email protected]). thin film shape alloy microactuators (TiNi Alloy Company, San Leandro, CA), silicon micro pumps (see M. Richter & J. Kruckow, aktorik/paper/2000Parkesbericht/ Paper2, 16.11.00), .
- air can be used to push liquid out of the reaction chamber or mix liquids within the reaction chamber. Whether the air pumps the fluid or bubbles through to generate a mixing effect is determine by the relative size of the bubble, the geometry of the chamber/channel and the surface tension of the liquid. Larger air-liquid interfaces tend to favor mixing over pumping. Mixing of liquid within the biochip cartridge can occur by pumping the liquid back and forth in the biochip cartridge.
- mixing is used to enhance hybridization rates.
- mixing is accomplished by inducing acoustic streaming using a piezo-electric transducer glued onto the back of the cartridge and excited with 5 Khz a.c. waveform at 10 V p _ p .
- mixing is accomplished by creating a thermal gradient across a chip.
- a thermal gradient may be created by heating the bottom of the chip to 65°C and cooling the top of the cartridge cover to 10°C. This can be accomplished by placing the chip between two pettier heaters, or by using an imbedded heater and a single peltier or other thermoelectric cooling devices.
- mixing is accomplished by recirculating liquid in a given chamber using an on chip or "off chip” pump attached to a chip.
- biochannel based mixing can be used to enhance hybridization rates.
- a bubble is intentionally introduced into one corner of the chip.
- mixing occurs as a result of the pressure flow created by changing the volume of the bubble within the chip.
- resonance induced mixing of bubbles can be done using PZT devices as well.
- mixing may be accomplished using non-contact mixing technologies like that describe by Covaris, Inc.
- heaters are incorporated onto or into the chip, to allow “on chip” heating (in addition, as described below, “off chip” thermocontrollers within the device may also be used).
- the reaction chamber is designed to maximize thermal conductivity between the chamber and the heater or thermocontroller.
- thermal mass i.e., making the surface of the chamber in contact with the heat source as thin as possible
- materials that are good thermal conductors i.e., metals
- thermally isolate the chamber from the rest of the chip are preferred.
- air pockets or vents are used to thermally isolate the amplificationchamber from the rest of the chip. That is, the there is a break in the continuity of the cartridge around the amplification chamber.
- thermally conductive materials are incorporated into or below the reaction chamber, forming hybrid chambers.
- a preferred embodiment utilizes one or more resistive heaters in the form of resistive metallic inks can be applied to a first layer of PC board. These heaters are powered by interconnects.
- a thin sheet of a thermally conductive material preferably a metal such as copper, is applied, to allow even heat distribution.
- the copper layer is then coated with a thin layer of biocompatible material, such as plastic. See Figure 10A.
- the total thickness of the hybrid chamber may vary from a few microns to millimeter dimension.
- a preferred thickness is approximately 200 microns.
- multiple thermal heaters are incorporated into the device to allow for the creation of multiple thermal zones.
- the temperature in the respective zones is maintained via either active or passive control. Frequently, thethermal connectivity of the cartridge materials are taken into account during the design.
- a chip may contain a thermal heater in the detection chamber of the cartridge in order to maintain the temperature of the detection chamber as well as constructing unique temperature zones in another part of device. In one embodiments, these temperature zones may be maintained to allow an enzymatic reaction to run efficiently. In another embodiment, multiple temperature zones may be maintained to simulate the temperatures normally used during PCR heat cycling. In order to effect the necessary temperature, the liquid can be maintained stationary and the temperature of the amplification chamber cycled (i.e. 95-55-72), alternatively, the liquid can be pumped over different temperature zones in order to obtain heat cycling (figure 10 B). This embodiment can be realized in different material substrates such as glass, plastic, ceramic and PCB.
- thermally insulative materials may be incorporated.
- thermal isolation may be accomplished by cutting out sections of the ceramic substrate such that solid regions of ceramic are separated from one another by a "cut out" as shown in Figure 10C.
- temperature sensors include the incorporation of temperature sensors into the substrate such that the temperature throughout the board can be monitored.
- temperature sensors are created using resistive devices, including silicon diodes.
- Other embodiments include the use of capillary thermostats and limiters (http://www.thermodisc.com/BulbAndCapillary.html).
- reaction chamber geometries which can be used in this way. Generally having the intersection of the inlet port and the reaction chamber be at the "bottom" of the cartridge, with a small aperture, with the reaction chamber widening, is preferred, ln addition, the "top" of the reaction chamber may narrow, as well.
- FIG 2. Several embodiments are depicted in Figure 2. Thus, preferred embodiments for the size and shape of the reaction chamber allow for smooth loading of the reaction chamber. Preferred embodiments utilize reaction chamber geometries that avoid the use of sharp corners or other components that serve as points for bubble formation.
- the reaction chamber can be configured to allow mixing of the sample.
- the inlet port and/or the reaction chamber can comprise weirs, channels or other components to maximize the mixing of the sample and reagent.
- the reaction may utilize magnetic beads for mixing and/or separation.
- the cartridge comprises a sealing and/or venting mechanism to prevent the cartridge from exploding due to a build up in pressure during a reaction, or to prevent leakage of the sample or reagents onto other parts of the substrate, particularly (in the case of electronic detection) onto electronic interconnects.
- a sealing and/or venting mechanism to prevent the cartridge from exploding due to a build up in pressure during a reaction, or to prevent leakage of the sample or reagents onto other parts of the substrate, particularly (in the case of electronic detection) onto electronic interconnects.
- this may take on a variety of different forms.
- there is a gasket between the biochip substrate comprising the array and the cartridge comprising sheets, tubes or strips.
- the housing may comprise an indentation or channel into which the gasket fits, and then the housing, gasket and chip are clamped together.
- adhesives can be used to attach the gasket to the cartridge, for example, a double sided adhesive can be used; for example, silicone, acrylic and combination adhesives can be used to attach the gasket to the biochip, which is then clamped into the cartridge as described herein.
- the reaction chamber and biochip substrate are configured such that a separate sealing mechanism is not required.
- the biochip substrate can serve as one "half of the reaction chamber, with the array on the inside, and the reaction chamber housing can serve as the other "half.
- the housing may encompass the substrate.
- Optional adhesives that may be used to seal the cartridge include, but are not limited to, pressure sensitive adhesives, thermal adhesives, etc.
- Other means of sealing the cartridges include sonic welding, laser bonding, and epoxys.
- the reaction chamber is made entirely of plastic.
- a PCB underlies all or a significant portion of the cartridge.
- the cartridge may be attached directly to the PCB.
- the device can be built wholly in the PCB, ceramic, or glass material with all of the necessary or a large majority of the necessary functions integrated into the device during the manufacturing process.
- the volume of the reaction chamber can be set either by forming a well in the cartridge, such that the addition of the biochip substrate forms a reaction chamber around the array, or by using a flat cartridge and using a gasket or adhesive of a defined depth, or by combinations of the three.
- the cartridge comprises a cap or lid.
- the cap may be functional, as outlined below when it comprises microfluidic components.
- the cap may be designed for safety purposes, to prevent the leakage of biological materials or cross-contamination.
- the cap can be designed to be removable.
- the cap can take on a wide variety of configurations.
- the cap merely seals the inlet port to prevent evaporation of the sample during the assay.
- the cap may comprise a number of additional elements for use in sample handling and reagent storage, to allow for a variety of different sample reactions.
- microfluidic components can be built into the cap to effect a number of manipulations on a sample to ultimately result in target analyte detection or quantitation. See generally PCT USOO/10903, and references outlined therein, all of which are expressly incorporated by reference.
- manipulations can include cell handling (cell concentration, cell lysis, cell removal, cell separation, etc.), separation of the desired target analyte from other sample components, chemical or enzymatic reactions on the target analyte, detection of the target analyte, etc.
- the devices of the invention can include one or more wells for sample manipulation, waste or reagents; microchannels (sometimes referred to as flow channels) to and between these wells, including microchannels containing electrophoretic separation matrices; valves to control fluid movement; on-chip pumps such as electroosmotic, electrohydrodynamic, or electrokinetic pumps.
- portions of the internal surfaces of the device may be coated with a variety of coatings as needed, to reduce non-specific binding, to allow the attachment of binding ligands, for biocompatibility, for flow resistance, etc.
- These microfluidic caps can be made in a variety of ways, as will be appreciated by those in the art. See for example references described in PCT USOO/10903, and references outlined therein, all of which are expressly incorporated by reference.
- the cap of the cartridge When the cap of the cartridge is used as part of the assay, it may be configured to include one or more of a variety of components, herein referred to as “modules”, that will be present on any given device depending on its use, and are connected as required by microchannels.
- These modules include, but are not limited to: sample inlet ports; sample introduction or collection modules; cell handling modules (for example, for cell lysis, cell removal, cell concentration, cell separation or capture, cell growth, etc.); separation modules, for example, for electrophoresis, dielectrophoresis, gel filtration, ion exchange/affinity chromatography (capture and release) etc.; reaction modules for chemical or biological alteration of the sample, including amplification of the target analyte (for example, when the target analyte is nucleic acid, amplification techniques are useful, including, but not limited to polymerase chain reaction (PCR), oligonucleotide ligation assay (OLA); strand displacement amplification (SDA), and nucleic acid sequence based amplification (NASBA) and other techniques outlined in WO 99/37819, PCT US00/19889, and US00/20476, all of which are hereby incorporated by reference in their entirety; chemical, physical or enzymatic cleavage or alter
- microfluidic components are described herein as being associated with the cap of the cartridge, as will be appreciated by those in the art, these modules and channels (as well as other components outlined herein) may be located anywhere in the cartridge or device.
- some components may be in the device; for example, “off chip” pumps may be located within one or more stations of the device.
- the cartridge comprises at least one biochip, with some embodiments utilizing one or more biochips per cartridge.
- biochip or equivalents herein is meant a substrate comprising an array of distinct biomolecules, particularly nucleic acids and proteins.
- nucleic acid biochips there are a wide variety of suitable nucleic acid biochips, including those made using photolithographic techniques (such as the Affymetrix GeneChipTM), spotting techniques (e.g. Synteni and Incyte), prining techniques (Agilent and Rosetta), three dimensional "gel pad” arrays, and those including electronic components (e.g. Nanogen).
- photolithographic techniques such as the Affymetrix GeneChipTM
- spotting techniques e.g. Synteni and Incyte
- prining techniques e.g. Synteni and Incyte
- three dimensional "gel pad” arrays e.g. Nanogen
- electronic components e.g. Nanogen
- one distinct advantage of the use of the electronic detection methods outlined herein is that real time monitoring of reactions and hybridization can occur. That is, while systems based on fluorescence require the removal of excess (e.g. unbound) signaling probes (or target sequences when the target sequence itself has been fluorescently labeled during an amplification reaction, for example), the electronic methods outlined herein do not. That is, unless the probes comprising the ETMs are bound to the surface, little or no signal is seen even if unbound probes have not been removed. This allows the monitoring of real-time reactions, as well as multiple measurements on the same array. Accordingly, while the discussion below is directed mainly to the use of biochips comprising an array of electrodes, other array technologies are included in the present invention.
- the biochips comprise substrates with a plurality of array locations.
- substrate or “solid support” or other grammatical equivalents herein is meant any material that can be modified to contain discrete individual sites appropriate of the attachment or association of capture ligands.
- Suitable substrates include metal surfaces such as gold, electrodes as defined below, glass and modified or functionalized glass, fiberglass, teflon, ceramics, mica, plastic (including acrylics, polystyrene and copolymers of styrene and other materials, polypropylene, polyethylene, polybutylene, polyimide, polycarbonate, polyurethanes, TeflonTM, and derivatives thereof, etc.), GETEK (a blend of polypropylene oxide and fiberglass), etc, polysaccharides, nylon or nitrocellulose, resins, silica or silica-based materials including silicon and modified silicon, carbon, metals, inorganic glasses and a variety of other polymers, with printed circuit board (PCB) materials being particularly preferred.
- PCB printed circuit board
- array herein is meant a plurality of capture ligands in an array format; the size of the array will depend on the composition and end use of the array. Arrays containing from about 2 different capture ligands to many thousands can be made. Generally, the array will comprise from two to as many as 100,000 or more, depending on the size of the electrodes, as well as the end use of the array. Preferred ranges are from about 2 to about 10,000, with from about 5 to about 1000 being preferred, and from about 10 to about 100 being particularly preferred.
- compositions of the invention may not be in array format; that is, for some embodiments, compositions comprising a single capture ligand may be made as well.
- multiple substrates may be used, either of different or identical compositions.
- large arrays may comprise a plurality of smaller substrates.
- the biochip comprises a substrate with at least one surface comprising an array, and in a preferred embodiment, an array of electrodes.
- electrode herein is meant a composition, which, when connected to an electronic device, is able to sense a current or charge and convert it to a signal.
- an electrode can be defined as a composition which can apply a potential to and/or pass electrons to or from species in the solution.
- an electrode is an ETM as described herein.
- Preferred electodes include, but are not limited to, certain metals and their oxides, including gold; platinum; palladium; silicon; aluminum; metal oxide electrodes including platinum oxide, titanium oxide, tin oxide, indium tin oxide, palladium oxide, silicon oxide, aluminum oxide, molybdenum oxide (Mo206), tungsten oxide (W03) and ruthenium oxides; and carbon (including glassy carbon electrodes, graphite and carbon paste).
- Preferred electrodes include gold, silicon, carbon and metal oxide electrodes, with gold being particularly preferred.
- the electrodes described herein are depicted as a flat surface, which is only one of the possible conformations of the electrode and is for schematic purposes only.
- the conformation of the electrode will vary with the detection method used and the configuration of the cartridge.
- flat planar electrodes may be preferred for optical detection methods, or when arrays of nucleic acids are made, thus requiring addressable locations for both synthesis and detection.
- the electrode may be in the form of a tube; this allows a maximum of surface area containing the nucleic acids to be exposed to a small volume of sample.
- the detection electrodes are formed on a substrate.
- the discussion herein is generally directed to the formation of gold electrodes, but as will be appreciated by those in the art, other electrodes can be used as well.
- the substrate can comprise a wide variety of materials, as outlined above.
- circuit board materials are those that comprise an insulating substrate that is coated with a conducting layer and processed using lithography techniques, particularly photolithography techniques, to form the patterns of electrodes and interconnects (sometimes referred to in the art as interconnections or leads).
- the insulating substrate is generally, but not always, a polymer.
- one or a plurality of layers may be used, to make either "two dimensional" (e.g. all electrodes and interconnections in a plane) or "three dimensional” (wherein the electrodes are on one surface and the interconnects may go through the board to the other side or wherein electrodes are on a plurality of surfaces) boards.
- Circuit board materials are often provided with a foil already attached to the substrate, such as a copper foil, with additional copper added as needed (for example for interconnections), for example by electroplating.
- the copper surface may then need to be roughened, for example through etching, to allow attachment of the adhesion layer.
- the present invention provides biochips (sometimes referred to herein "chips") that comprise substrates comprising a plurality of electrodes, preferably gold electrodes.
- the number of electrodes is as outlined for arrays.
- Each electrode preferably comprises a self-assembled monolayer as outlined herein.
- one of the monolayer- forming species comprises a capture ligand as outlined herein.
- each electrode has an interconnection, that is attached to the electrode at one end and is ultimately attached to a device that can control the electrode. That is, each electrode is independently addressable.
- the connections from the electrodes are made by passing through the substrate to produce a so called land grid array that can interface to a pogo pin or like connector to make connections from the chip to the instrument.
- pogo pin connectors are used in place of edge card connectors.
- FIG 1 H?? An example of a chip containing electrodes arranged in a land grid array is shown in Figure 1 H??.
- the electrode array is one surface of the substrate, such as a PCR board or ceramic substrate, and there are "through board” or "through substrate” interconnects ending in pads. See Figure 11??.
- switching circuitry can be built into the pogo pin connector.
- Detection electrodes on circuit board material are generally prepared in a wide variety of ways.
- high purity gold is used, and it may be deposited on a surface via vacuum deposition processes (sputtering and evaporation) or solution deposition (electroplating or electroless processes).
- the substrate When electroplating is done, the substrate must initially comprise a conductive material; fiberglass circuit boards are frequently provided with copper foil.
- an adhesion layer between the substrate and the gold in order to insure good mechanical stability is used.
- preferred embodiments utilize a deposition layer of an adhesion metal such as chromium, titanium, titanium/tungsten, tantalum, nickel or palladium, which can be deposited as above for the gold.
- grain refining additives When electroplated metal (either the adhesion metal or the electrode metal) is used, grain refining additives, frequently referred to in the trade as brighteners, can optionally be added to alter surface deposition properties.
- Preferred brighteners are mixtures of organic and inorganic species, with cobalt and nickel being preferred.
- the adhesion layer is from about 100 A thick to about 25 microns (1000 microinches).
- the electrode metal preferably gold
- the electrode metal is deposited at thicknesses ranging from about 500 A to about 5 microns (200 microinches), with from about 30 microinches to about 50 microinches being preferred.
- the gold is deposited to make electrodes ranging in size from about 5 microns to about 5 mm in diameter, with about 100 to 250 microns being preferred.
- the detection electrodes thus formed are then preferably cleaned and SAMs added, as is discussed below.
- the present invention provides methods of making a substrate comprising a plurality of gold electrodes.
- the methods first comprise coating an adhesion metal, such as nickel or palladium (optionally with brightener), onto the substrate. Electroplating is preferred.
- the electrode metal preferably gold, is then coated (again, with electroplating preferred) onto the adhesion metal.
- the patterns of the device, comprising the electrodes and their associated interconnections are made using lithographic techniques, particularly photolithographic techniques as are known in the art, and wet chemical etching.
- a non-conductive chemically resistive insulating material such as solder mask or plastic is laid down using these photolithographic techniques, leaving only the electrodes and a connection point to the leads exposed; the leads themselves are generally coated.
- the solder mask is desirably made of a solvent soluble material rather than a water soluble material.
- Water soluble solder masks have become standard in the industry because of the environmental advantages of water soluble materials generally. Unfortunately, for a detector chip that is to be exposed to aqueous solutions, water soluble materials such as for example acetonitrile can dissolve when exposed to aqueous solution.
- drop deposition techniques are used to add the required chemistry, i.e. the monolayer forming species, one of which is preferably a capture ligand comprising species.
- Drop deposition techniques are well known for making "spot" arrays. This is done to add a different composition to each electrode, i.e. to make an array comprising different capture ligands.
- the SAM species may be identical for each electrode, and this may be accomplished using a drop deposition technique or the immersion of the entire substrate or a surface of the substrate into the solution.
- plasma treatments are used to generate a surface free of major contaminants prior to the deposition of SAMs comprising capture probes. This method is particularly useful for the activation of gold surfaces for the formation of SAMs comprising capture probes with packing densities close to the theoretical limit (see Figure 68). Plasma methods can also be used for the deposition of different capture probes on neighboring pads.
- Plasma treatment in a barrel type machine (minimal ion bombardment) with oxygen plasma is commonly used in semiconductor processing to remove trace residues of organic contaminants, including photoresistant contaminants.
- oxygen plasma can be used in the methods of the present invention for generating a clean surface, this treatment makes the insulator layer separating the gold pads hydrophilic. Thus, it is difficult to spot arrays without contamination-
- a hydrogen plasma treatment is used. This procedure recovers hydrophobicity on organic surfaces because it converts hydrophilic C-O bonds to C-H bonds. In addition, this treatment does not add contaminants to the gold surface. Hydrogen plasma treatment can be used alone, or in combination with an oxygen plasma treatment.
- Figure 69 illustrates the effectiveness of an oxygen plasma treatment followed by a hydrogen plasma treatment for removing major contaminants from chips.
- Combining an oxygen plasma treatment with a hydrogen plasma treatment can be used on micro- patterned photoresistant materials to generate hydrophobic surfaces next to hydrophilic surfaces.
- the hydrophobic and hydrophilic surfaces can either be adjacent to each other or separated by a few microns.
- CF 4 plasma can be used after an oxygen plasma treatment to make teflonTM-like compounds, i.e. C-F bonds, on the insulator, resulting in a hydrophobic insulator surface.
- a chemical treatment can be combined with a plasma treatment.
- chemical treatment with silanes can be used to make the oxide insulator surface hydrophobic or hydrophilic, while leaving non-oxide surfaces, such as gold, uncontaminated. Whether the insulator surface is hydrophobic or hydrophilic depends on the type of silane that replaces the O-H bonds. Additionally, this procedure can be used in conjunctions with plasma cleaning to enable selective wetting of chemical and biological fluids on the chip surface or to prevent or allow sticking of a given species of solution to the surface of the chip.
- the biochips comprise electrodes
- additional components in addition to the chemistry outlined below, which may be present on the chip, including, but not limited to, interconnects, multiplexers, relay devices, filters, RF antennae, heating elements, electromagnetic ' components, etc.
- Each electrode comprises an independent lead (interconnect) to transmit input and electronic response signals for each electrode of the array.
- interconnect an independent lead to transmit input and electronic response signals for each electrode of the array.
- each electrode is individually connected to a corresponding input of a multiplexer via a corresponding interconnector.
- One problem presented in conventional systems and methods is the difficulty in providing electrical connections (inputs and/or outputs) to a large number of electrodes, particularly if the electrodes form a dense or close packed array.
- Several solutions to this problem have been identified, and include the use of circuitry that allows signal processing either simultaneously as sets of parallel circuits and connections, line-sample array addressing, serially in a time-domain multiplexed manner, or in parallel or serially using frequency domain and/or time-domain based separation techniques, among other available techniques, as are outlined herein.
- a preferred method to connect a first multiplicity of circuits or lines on the chip to a smaller plurality of lines at a connector leading from the chip are to use a switching device such as a multiplexer (MUX) or relays to selectively couple circuits on the chip or board with circuits off the board.
- a switching device such as a multiplexer (MUX) or relays to selectively couple circuits on the chip or board with circuits off the board.
- MUX multiplexer
- the number of multiplexers will depend on the number of electrodes in the array.
- a single MUX is utilized.
- a plurality of MUXs are used. This can be done in a variety of ways, as will be appreciated by those in the art; in one embodiment, "sectors" of electrodes are assigned to a particular MUX; thus for example, rows or columns of the array may each have their own MUX.
- submultiplexers are used; for example, a column or row is connected to a respective sub-multiplexer, with the sub-multiplexer outputs going to another submultiplexer.
- the multiplexer includes a binary counter which receives the control signal via the connector pad.
- the control signal is preferably a pulsed signal such as a clock signal and generates a sequential count to drive the decoders.
- another way to connect a multiplicity of electrodes on the substrate to a smaller number of connector pads leading "off chip” is to use row-column select signals to allow the selection of individual electrodes.
- Diffusion rates may play a more important role than when the reaction occurs in solution. It is important to understand when or over what period of time the reaction takes place so that the measurements are taken at the appropriate time. This may be particularly important if an intermediate reaction product is to be sensed, or if a series of measurements are desirable, for example to do reaction kinetics.
- Reaction kinetics are also an important consideration for the driving signals. Biosensors are limited by the chemical kinetics.
- each molecule has a maximum speed or velocity in the medium.
- the molecules may typically be actively driven or moved in solution at frequencies between about 1 Hz and 10kHz, more typically between about 5 Hz and 5 kHz. At higher frequencies, the molecules only vibrate, while at lower frequencies the movement is not particularly useful.
- an assay volume that is the accessible volume of the assay, associated with each " driving signal frequency. As the frequency increases, the assay volume shrinks in size and volume. This has implication for the distribution of electrodes and the driving signal frequency.
- reaction medium such as solution components, sample components, reaction components, etc.
- the electrodes will degrade, become passivated, or otherwise change over time thereby affecting the accuracy and uniformity of measurements. Under such conditions it is desirable to perform the sensing, measurement, or analysis quickly, or at least according to predetermined timings so that the data collected will be properly interpreted.
- one or more preamplifiers are used.
- the preamplifier can be on the surface of the substrate, e.g. "on board” or “on chip”, or may be provided in circuitry external to the array chip. It is preferable, however, that the preamplifier be included on the substrate to increase the signal-to-noise ratio of the signal provided to the external circuitry.
- each individual electrode has an associated preamplifier.
- the array is divided into "sectors", wherein a subset of the electrodes in the array have an associated MUX and preamplifier.
- other components of the invention may be associated with sectors.
- impedance matching is done.
- filters are used, including, but not limited to, time domain filters and frequency domain filters, and combinations.
- the electrodes of the invention in preferred embodiments comprise self-assembled monolayers (SAMs).
- SAMs self-assembled monolayers
- the compositions of these SAMs will vary with the detection method used. In general, there are two basic detection mechanisms. In a preferred embodiment, detection of an ETM is based on electron transfer through the stacked ⁇ -orbitals of double stranded nucleic acid. This basic mechanism is described in U.S. Patent Nos. 5,591,578, 5,770,369, 5,705,348, and PCT US97/20014 and is termed "mechanism-1" herein.
- the ETM can be detected, not necessarily via electron transfer through nucleic acid, but rather can be directly detected on an electrode comprising a SAM; that is, the electrons from the ETMs need not travel through the stacked ⁇ orbitals in order to generate a signal.
- the detection electrode preferably comprises a self-assembled monolayer (SAM) that serves to shield the electrode from redox-active species in the sample.
- SAM self-assembled monolayer
- the electroconduits allow particular ETMs access to the surface.
- the configuration of the electroconduit depends in part on the ETM chosen.
- the use of relatively hydrophobic ETMs allows the use of hydrophobic electroconduit forming species, which effectively exclude hydrophilic or charged ETMs.
- the use of more hydrophilic or charged species in the SAM may serve to exclude hydrophobic ETMs.
- the electroconduits can be generated in several general ways, including but not limited to the use of rough electrode surfaces, such as gold electrodes formulated on PC circuit boards; or the inclusion of at least two different species in the monolayer, i.e. using a "mixed monolayer", at least one of which is a electroconduit-forming species (EFS).
- ETM electroconduit-forming species
- the role of the SAM comprising the defects is to allow electronic contact of the ETM with the electronic surface of the electrode, while still providing the benefits of shielding the electrode from solution components and reducing the amount of non-specific binding to the electrodes.
- the role of the binding ligand is to provide specificity for a recruitment of ETMs to the surface, where they can be directly detected.
- an assay complex is formed that contains an ETM, which is then detected using the detection electrode.
- the electrode comprises a monolayer, comprising electroconduit forming species (EFS).
- EFS electroconduit forming species
- the efficiency of target analyte binding may increase when the analyte is at a distance from the electrode.
- non-specific binding of biomolecules, including the target analytes, to an electrode is generally reduced when a monolayer is present.
- a monolayer facilitates the maintenance of the analyte away from the electrode surface.
- a monolayer serves to keep charged species away from the surface of the electrode. Thus, this layer helps to prevent electrical contact between the electrodes and the ETMs, or between the electrode and charged species within the solvent.
- the monolayer is preferably tightly packed in a uniform layer on the electrode surface, such that a minimum of "holes" exist.
- the monolayer thus serves as a physical barrier to block solvent community to the electrode.
- monolayer or “self-assembled monolayer” or “SAM” herein is meant a relatively ordered assembly of molecules spontaneously chemisorbed on a surface, in which the molecules are oriented approximately parallel to each other and roughly perpendicular to the surface. A majority of the molecules include a functional group that adheres to the surface, and a portion that interacts with neighboring molecules in the monolayer to form the relatively ordered array.
- a “mixed” monolayer comprises a heterogeneous monolayer, that is, where at least two different molecules make up the monolayer.
- the SAMs of the invention can be generated in a number of ways and comprise a number of different components, depending on the electrode surface and the system used.
- preferred embodiments utilize two monolayer forming species: a monolayer forming species (including insulators or conductive oligomers) and a conductive oligomer species comprising the capture binding ligand, although as will be appreciated by those in the art, additional monolayer forming species can be included as well.
- the composition of the SAM depends on the detection electrode surface.
- detection electrodes comprising "smooth” surfaces, such as gold ball electrodes
- those comprising "rough” surfaces such as those that are made using commercial processes on PC circuit boards.
- monolayers made on imperfect surfaces i.e. "rough” surfaces
- spontaneously form monolayers containing enough electroconduits even in the absence of EFS probably due to the fact that the formation of a uniform monolayer on a rough surface is difficult.
- “Smoother” surfaces may require the inclusion of sufficient numbers of EFS to generate the electroconduits, as the uniform surfaces allow a more uniform monolayer to form.
- “smooth” surfaces comprise monolayers comprising three components: an insulator species, a EFS, and a species comprising the capture ligand, although in some circumstances, for example when the capture ligand species is included at high density, the capture ligand species can serve as the EFS.
- “Smoothness” in this context is not measured physically but rather as a function of an increase in the measured signal when EFS are included. That is, the signal from a detection electrode coated with monolayer forming species is compared to a signal from a detection electrode coated with monolayer forming species including a EFS.
- electroconduits do not result in direct contact of sample components with the electrode surface; that is, the electroconduits are not large pores or holes that allow physical access to the electrode. Rather, without being bound by theory, it appears that the electroconduits allow certain types of ETMs, particularly hydrophobic ETMs, to penetrate sufficiently into the monolayer to allow detection. However, other types of redox active species, including some hydrophilic species, do not penentrate into the monolayer, even with electroconduits present. Thus, in general, redox active species that may be present in the sample do not give substantial signals as a result of the electroconduits.
- the test for a suitable SAM to reduce non-specific binding that also has sufficient electroconduits for ETM detection is to add either ferrocene or ferrocyanide to the SAM; the former should give a signal and the latter should not.
- the monolayer comprises a first species comprising a conductive oligomer comprising the capture binding ligand, as is more fully outlined below, and a second species comprising a monolayer forming species, including either or both insulators or conductive oligomers.
- the monolayer comprises electroconduit-forming species.
- electroconduit-forming species or “EFS” herein is meant a molecule that is capable of generating sufficient electroconduits in a monolayer, generally of insulators such as alkyl groups, to allow detection of ETMs at the surface.
- EFSs have one or more of the following qualities: they may be relatively rigid molecules, for example as compared to an alkyl chain; they may attach to the electrode surface with a geometry different from the other monolayer forming species (for example, alkyl chains attached to gold surfaces with thiol groups are thought to attach at roughly 45° angles, and phenyl-acetylene chains attached to gold via thiols are thought to go down at 90° angles); they may have a structure that sterically interferes or interrupts the formation of a tightly packed monolayer, for example through the inclusion of branching groups such as alkyl groups, or the inclusion of highly flexible species, such as polyethylene glycol units; or they may be capable of being activated to form electroconduits; for example, photoactivatible species that can be selectively removed from the surface upon photoactivation, leaving electroconduits.
- EFSs include conductive oligomers, as defined below, and phenyl-acetylene-polyethylene glycol species, as well as asymmetrical SAM-forming disulfide species such as described in U.S.S.N. 09/847,113, filed May 1, 2001, hereby expressly incorporated by reference.
- the EFS is not a conductive oligomer.
- the monolayer comprises conductive oligomers.
- conductive oligomer herein is meant a substantially conducting oligomer, preferably linear, some embodiments of which are referred to in the literature as “molecular wires”.
- substantially conducting herein is meant that the oligomer is capable of transferring electrons at 100 Hz.
- the conductive oligomer has substantially overlapping ⁇ -orbitals, i.e. conjugated ⁇ -orbitals, as between the monomeric units of the conductive oligomer, although the conductive oligomer may also contain one or more sigma ( ⁇ ) bonds.
- a conductive oligomer may be defined functionally by its ability to inject or receive electrons into or from an associated ETM. Furthermore, the conductive oligomer is more conductive than the insulators as defined herein. Additionally, the conductive oligomers of the invention are to be distinguished from electroactive polymers, that themselves may donate or accept electrons.
- the conductive oligomers have a conductivity, S, of from between about 10 "6 to about 10 4 ⁇ "1 cm “1 , with from about 10 "5 to about 10 3 ⁇ "1 cn ⁇ 1 being preferred, with these S values being calculated for molecules ranging from about 2 ⁇ A to about 20 ⁇ A.
- insulators have a conductivity S of about 10 "7 ⁇ "1 cm “1 or lower, with less than about 10 "8 ⁇ "1 cm “1 being preferred. See generally Gardner et al., Sensors and Actuators A 51 (1995) 57-66, incorporated herein by reference.
- Desired characteristics of a conductive oligomer include high conductivity, sufficient solubility in organic solvents and/or water for synthesis and use of the compositions of the invention, and preferably chemical resistance to reactions that occur i) during nucleic acid synthesis (such that nucleosides containing the conductive oligomers may be added to a nucleic acid synthesizer during the synthesis of the compositions of the invention), ii) during the attachment of the conductive oligomer to an electrode, or iii) during hybridization assays.
- conductive oligomers that will promote the formation of self-assembled monolayers are preferred.
- oligomers of the invention comprise at least two monomeric subunits, as described herein. As is described more fully below, oligomers include homo- and hetero-oligomers, and include polymers.
- the conductive oligomer has the structure depicted in Structure 1: Structure 1
- the conductive oligomer of Structure 1 may be attached to ETMs, such as electrodes, transition metal complexes, organic ETMs, and metallocenes, and to nucleic acids, or to several of these.
- ETMs such as electrodes, transition metal complexes, organic ETMs, and metallocenes
- nucleic acids or to several of these.
- the conductive oligomers depicted herein will be attached at the left side to an electrode; that is, as depicted in Structure 1, the left “Y” is connected to the electrode as described herein. If the conductive oligomer is to be attached to a nucleic acid, the right "Y", if present, is attached to the nucleic acid, either directly or through the use of a linker, as is described herein.
- Y is an aromatic group
- n is an integer from 1 to 50
- g is either 1 or zero
- e is an integer from zero to 10
- m is zero or 1.
- B-D is a bond able to conjugate with neighboring bonds (herein referred to as a "conjugated bond”), preferably selected from acetylene
- D is preferably carbonyl, or a heteroatom moiety, wherein the heteroatom is selected from oxygen, sulfur, nitrogen, silicon or phosphorus.
- suitable heteroatom moieties include, but are not limited to, -NH and -NR, wherein R is as defined herein; substituted sulfur; sulfonyl (-S0 2 -) sulfoxide (-SO-); phosphine oxide (-PO- and -RPO-); and thiophosphine (-PS- and -RPS-).
- sulfur derivatives are not preferred.
- aromatic group or grammatical equivalents herein is meant an aromatic monocyclic or polycyclic hydrocarbon moiety generally containing 5 to 14 carbon atoms (although larger polycyclic rings structures may be made) and any carbocylic ketone or thioketone derivative thereof, wherein the carbon atom with the free valence is a member of an aromatic ring.
- Aromatic groups include arylene groups and aromatic groups with more than two atoms removed. For the purposes of this application aromatic includes heterocycle.
- Heterocycle or “heteroaryl” means an aromatic group wherein 1 to 5 of the indicated carbon atoms are replaced by a heteroatom chosen from nitrogen, oxygen, sulfur, phosphorus, boron and silicon wherein the atom with the free valence is a member of an aromatic ring, and any heterocyclic ketone and thioketone derivative thereof.
- heterocycle includes thienyl, . furyl, pyrrolyl, pyrimidinyl, oxalyl, indolyl, purinyl, quinolyl, isoquinolyl, thiazolyl, imidozyl, etc.
- the Y aromatic groups of the conductive oligomer may be different, i.e. the conductive oligomer may be a heterooligomer. That is, a conductive oligomer may comprise a oligomer of a single type of Y groups, or of multiple types of Y groups.
- the aromatic group may be substituted with a substitution group, generally depicted herein as R.
- R groups may be added as necessary to affect the packing of the conductive oligomers, i.e. R groups may be used to alter the association of the oligomers in the monolayer. R groups may also be added to 1 ) alter the solubility of the oligomer or of compositions containing the oligomers; 2) alter the conjugation or electrochemical potential of the system; and 3) alter the charge or characteristics at the surface of the monolayer.
- R groups are preferred to increase solubility when solution synthesis is done.
- the R groups, and their positions, are chosen to minimally effect the packing of the conductive oligomers on a surface, particularly within a monolayer, as described below.
- only small R groups are used within the monolayer, with larger R groups generally above the surface of the monolayer.
- attachment of methyl groups to the portion of the conductive oligomer within the monolayer to increase solubility is preferred, with attachment of longer alkoxy groups, for example, C3 to C10, is preferably done above the monolayer surface.
- this generally means that attachment of sterically significant R groups is not done on any of the first two or three oligomer subunits, depending on the average length of the molecules making up the monolayer.
- R groups include, but are not limited to, hydrogen, alkyl, alcohol, aromatic, amino, amido, nitro, ethers, esters, aldehydes, sulfonyl, silicon moieties, halogens, sulfur containing moieties, phosphorus containing moieties, and ethylene glycols.
- R is hydrogen when the position is unsubstituted. It should be noted that some positions may allow two substitution groups, R and R', in which case the R and R' groups may be either the same or different.
- alkyl group or grammatical equivalents herein is meant a straight or branched chain alkyl group, with straight chain alkyl groups being preferred. If branched, it may be branched at one or more positions, and unless specified, at any position.
- the alkyl group may range from about 1 to about 30 carbon atoms (C1 -C30), with a preferred embodiment utilizing from about 1 to about 20 carbon atoms (C1 -C20), with about C1 through about C12 to about C15 being preferred, and C1 to C5 being particularly preferred, although in some embodiments the alkyl group may be much larger.
- alkyl group also included within the definition of an alkyl group are cycloalkyl groups such as C5 and C6 rings, and heterocyclic rings with nitrogen, oxygen, sulfur or phosphorus.
- Alkyl also includes heteroalkyl, with heteroatoms of sulfur, oxygen, nitrogen, and silicone being preferred.
- Alkyl includes substituted alkyl groups.
- substituted alkyl group herein is meant an alkyl group further comprising one or more substitution moieties "R", as defined above.
- amino groups or grammatical equivalents herein is meant -NH 2 , -NHR and -NR 2 groups, with R being as defined herein.
- nitro group herein is meant an -N0 2 group.
- sulfur containing moieties herein is meant compounds containing sulfur atoms, including but not limited to, thia-, thio- and sulfo- compounds, thiols (-SH and -SR), and sulfides (-RSR-).
- phosphorus containing moieties herein is meant compounds containing phosphorus, including, but not limited to, phosphines and phosphates.
- silicon containing moieties herein is meant compounds containing silicon.
- ether herein is meant an -O-R group.
- Preferred ethers include alkoxy groups, with -0-(CH 2 ) 2 CH 3 and -0-(CH 2 ) 4 CH 3 being preferred.
- esters herein is meant a -COOR group.
- halogen herein is meant bromine, iodine, chlorine, or fluorine.
- Preferred substituted alkyls are partially or fully halogenated alkyls such as CF 3 , etc.
- aldehyde herein is meant -RCHO groups.
- alcohol herein is meant -OH groups, and alkyl alcohols -ROH.
- ethylene glycol or "(poly)ethylene glycol” herein is meant a -(0-CH 2 -CH 2 ) n - group, although each carbon atom of the ethylene group may also be singly or doubly substituted, e.g. -(0-CR 2 -CR 2 ) n -, with R as described above.
- Ethylene glycol derivatives with other heteroatoms in place of oxygen i.e. -(N- CH 2 -CH 2 ) n - or -(S-CH 2 -CH 2 ) n -, or with substitution groups are also preferred.
- substitution groups include, but are not limited to, methyl, ethyl, propyl, alkoxy groups such as -0-(CH 2 ) 2 CH 3 and -0-(CH 2 ) 4 CH 3 and ethylene glycol and derivatives thereof.
- Preferred aromatic groups include, but are not limited to, phenyl, naphthyl, naphthalene, anthracene, phenanthroline, pyrole, pyridine, thiophene, porphyrins, and substituted derivatives of each of these, included fused ring derivatives.
- B-D is a bond linking two atoms or chemical moieties.
- B-D is a conjugated bond, containing overlapping or conjugated ⁇ -orbitals.
- B-D bonds are acetylene, alkene, amide, and substituted derivatives of these three, and azo.
- Especially preferred B-D bonds are acetylene, alkene and amide.
- the oligomer components attached to double bonds may be in the trans or cis conformation, or mixtures.
- B or D may include carbon, nitrogen or silicon.
- the substitution groups are as defined as above for R.
- e is preferably 1 and the D moiety may be carbonyl or a heteroatom moiety as defined above.
- the terminal B-D bond may be an amide bond
- the rest of the B-D bonds may be acetylene bonds.
- amide bonds when amide bonds are present, as few amide bonds as possible are preferable, but in some embodiments all the B-D bonds are amide bonds.
- one type of B-D bond may be present in the conductive oligomer within a monolayer as described below, and another type above the monolayer level, for example to give greater flexibility for nucleic acid hybridization when the nucleic acid is attached via a conductive oligomer.
- n is an integer from 1 to 50, although longer oligomers may also be used (see for example Schumm et al., Angew. Chem. Int. Ed. Engl. 1994 33(13): 1360). Without being bound by theory, it appears that for efficient hybridization of nucleic acids on a surface, the hybridization should occur at a distance from the surface, i.e. the kinetics of hybridization increase as a function of the distance from the surface, particularly for long oligonucleotides of 200 to 300 basepairs.
- the length of the conductive oligomer is such that the closest nucleotide of the nucleic acid is positioned from about 6A to about 10 ⁇ A (although distances of up to 500A may be used) from the electrode surface, with from about 15A to about.6 ⁇ A being preferred and from about 25A to about 6 ⁇ A also being preferred.
- n will depend on the size of the aromatic group, but generally will be from about 1 to about 20, with from about 2 to about 15 being preferred and from about 3 to about 10 being especially preferred.
- m is either 0 or 1. That is, when m is 0, the conductive oligomer may terminate in the B-D bond or D moiety, i.e. the D atom is attached to the nucleic acid either directly or via a linker. In some embodiments, for example when the conductive oligomer is attached to a phosphate of the ribose-phosphate backbone of a nucleic acid, there may be additional atoms, such as a linker, attached between the conductive oligomer and the nucleic acid. Additionally, as outlined below, the D atom may be the nitrogen atom of the amino-modified ribose. Alternatively, when m is 1, the conductive oligomer may terminate in Y, an aromatic group, i.e. the aromatic group is attached to the nucleic acid or linker.
- conductive oligomers may be utilized. These include conductive oligomers falling within the Structure 1 and Structure 8 formulas, as well as other conductive oligomers, as are generally known in the art, including for example, compounds comprising fused aromatic rings or Teflon®-like oligomers, such as -(CF 2 ) n -, -(CHF) n - and -(CFR) n -. See for example, Schumm et al., Angew. Chem. Intl. Ed. Engl. 33:1361 (1994); Grosshenny et al., Platinum Metals Rev. 40(1):26-35 (1996); Tour, Chem. Rev. 96:537-553 (1996); Hsung et al., Organometallics 14:4808-4815 (1995); and references cited therein, all of which are expressly incorporated by reference.
- Structure 2 is Structure 1 when g is 1.
- Preferred embodiments of Structure 2 include: e is zero, Y is pyrrole or substituted pyrrole; e is zero, Y is thiophene or substituted thiophene; e is zero, Y is furan or substituted furan; e is zero, Y is phenyl or substituted phenyl; e is zero, Y is pyridine or substituted pyridine; e is 1, B-D is acetylene and Y is phenyl or substituted phenyl (see Structure 4 below).
- a preferred embodiment of Structure 2 is also when e is one, depicted as Structure 3 below:
- Preferred embodiments of Structure 3 are: Y is phenyl or substituted phenyl and B-D is azo; Y is phenyl or substituted phenyl and B-D is acetylene; Y is phenyl or substituted phenyl and B-D is alkene; Y is pyridine or substituted pyridine and B-D is acetylene; Y is thiophene or substituted thiophene and B-D is acetylene; Y is furan or substituted furan and B-D is acetylene; Y is thiophene or furan (or substituted thiophene or furan) and B-D are alternating alkene and acetylene bonds.
- Structure 3 conductive oligomer Most of the structures depicted herein utilize a Structure 3 conductive oligomer. However, any Structure 3 oligomers may be substituted with any of the other structures depicted herein, i.e. Structure 1 or 8 oligomer, or other conducting oligomer, and the use of such Structure 3 depiction is not meant to limit the scope of the invention.
- Particularly preferred embodiments of Structure 4 include: n is two, m is one, and R is hydrogen; n is three, m is zero, and R is hydrogen; and the use of R groups to increase solubility.
- the conductive oligomers are pseudopeptide oligomers.
- the amide bond in Structure 5 is depicted with the carbonyl to the left, i.e. - CONH-, the reverse may also be used, i.e. -NHCO-.
- Particularly preferred embodiments of Structure 5 include: n is two, m is one, and R is hydrogen; n is three, m is zero, and R is hydrogen (in this embodiment, the terminal nitrogen (the D atom) may be the nitrogen of the amino-modified ribose); and the use of R groups to increase solubility.
- Preferred embodiments of Structure 6 include the first n is two, second n is one, m is zero, and all R groups are hydrogen, or the use of R groups to increase solubility.
- Preferred embodiments of Structure 7 include: the first n is three, the second n is from 1-3, with m being either 0 or 1 , and the use of R groups to increase solubility.
- the conductive oligomer has the structure depicted in Structure 8:
- C are carbon atoms
- n is an integer from 1 to 50
- m is 0 or 1
- J is a heteroatom selected from the group consisting of oxygen, nitrogen, silicon, phosphorus, sulfur, carbonyl or sulfoxide
- the G bond of each subunit may be the same or different than the G bonds of other subunits; that is, alternating oligomers of alkene and acetylene bonds could be used, etc.
- G is an alkane bond
- the number of alkane bonds in the oligomer should be kept to a minimum, with about six or less sigma bonds per conductive oligomer being preferred.
- Alkene bonds are preferred, and are generally depicted herein, although alkane and acetylene bonds may be substituted in any structure or embodiment described herein as will be appreciated by those in the art.
- the m of Structure 8 is zero. In a particularly preferred embodiment, the m of Structure 8 is zero.
- n is zero and G is an alkene bond, as is depicted in Structure 9:
- alkene oligomer of structure 9, and others depicted herein, are generally depicted in the preferred trans configuration, although oligomers of cis or mixtures of trans and cis may also be used.
- R groups may be added to alter the packing of the compositions on an electrode, the hydrophilicity or hydrophobicity of the oligomer, and the flexibility, i.e. the rotational, torsional or longitudinal flexibility of the oligomer.
- n is as defined above.
- R is hydrogen, although R may be also alkyl groups and polyethylene glycols or derivatives.
- the conductive oligomer may be a mixture of different types of oligomers, for example of structures 1 and 8.
- the terminus of at least some of the conductive oligomers in the monolayer are electronically exposed.
- electroly exposed herein is meant that upon the placement of an ETM in close proximity to the terminus, and after initiation with the appropriate signal, a signal dependent on the presence of the ETM may be detected.
- the conductive oligomers may or may not have terminal groups. Thus, in a preferred embodiment, there is no additional terminal group, and the conductive oligomer terminates with one of the groups depicted in Structures 1 to 9; for example, a B-D bond such as an acetylene bond. Alternatively, in a preferred embodiment, a terminal group is added, sometimes depicted herein as "Q".
- a terminal group may be used for several reasons; for example, to contribute to the electronic availability of the conductive oligomer for detection of ETMs, or to alter the surface of the SAM for other reasons, for example to prevent non-specific binding.
- Preferred terminal groups include -NH 2 , -OH, -COOH, and alkyl groups such as -CH 3 , and (poly)alkyloxides such as (poly)ethylene glycol, with -OCH 2 CH 2 OH, -(OCH 2 CH 2 0) 2 H, -(OCH 2 CH 2 0) 3 H, and -(0CH 2 CH 2 0) 4 H being preferred.
- the terminal groups may facilitate detection, and some may prevent non-specific binding.
- the monolayer may comprise different conductive oligomer species, although preferably the different species are chosen such that a reasonably uniform SAM can be formed.
- the monolayer may comprise different conductive oligomer species, although preferably the different species are chosen such that a reasonably uniform SAM can be formed.
- nucleic acids are covalently attached to the electrode using conductive oligomers
- preferred embodiments utilize conductive oligomers that terminate below the surface of the rest of the monolayer, i.e. below the insulator layer, if used, or below some fraction of the other conductive oligomers.
- the use of different conductive oligomers may be done to facilitate monolayer formation, or to make monolayers with altered properties.
- the monolayer forming species are "interrupted" conductive oligomers, containing an alkyl portion in the middle of the conductive oligomer.
- the monolayer comprises photoactivatable species as EFSs.
- EFSs photoactivatable species
- This general scheme is depicted in Figure 11 of 09/626,096, incorporated by reference.
- Photoactivatable species are known in the art, and include 4,5-dimethoxy-2-nitrobenzyl ester, which can be photolyzed at 365 nm for 2 hours.
- the monolayer may further comprise insulator moieties.
- insulator herein is meant a substantially nonconducting oligomer, preferably linear.
- substantially nonconducting herein is meant that the insulator will not transfer electrons at 100 Hz. The rate of electron transfer through the insulator is preferably slower than the rate through the conductive oligomers described herein.
- the insulators have a conductivity, S, of about 10 '7 ⁇ "1 c ⁇ r 1 or lower, with less than about 10 "8 ⁇ "1 C ⁇ Y 1 being preferred. See generally Gardner et al., supra.
- insulators are alkyl or heteroalkyl oligomers or moieties with sigma bonds, although any particular insulator molecule may contain aromatic groups or one or more conjugated bonds.
- heteroalkyl herein is meant an alkyl group that has at least one heteroatom, i.e. nitrogen, oxygen, sulfur, phosphorus, silicon or boron included in the chain.
- the insulator may be quite similar to a conductive oligomer with the addition of one or more heteroatoms or bonds that serve to inhibit or slow, preferably substantially, electron transfer.
- Suitable insulators include, but are not limited to, -(CH 2 ) n -, -(CRH) n -, and - (CR 2 ) n -, ethylene glycol or derivatives using other heteroatoms in place of oxygen, i.e. nitrogen or sulfur (sulfur derivatives are not preferred when the electrode is gold).
- the insulators may be substituted with R groups as defined herein to alter the packing of the moieties or conductive oligomers on an electrode, the hydrophilicity or hydrophobicity of the insulator, and the flexibility, i.e. the rotational, torsional or longitudinal flexibility of the insulator.
- R groups as defined herein to alter the packing of the moieties or conductive oligomers on an electrode, the hydrophilicity or hydrophobicity of the insulator, and the flexibility, i.e. the rotational, torsional or longitudinal flexibility of the insulator.
- branched alkyl groups may be used.
- the insulators may contain terminal groups, as outlined above, particularly to influence the surface of the monolayer.
- the insulator species included in the SAM utilizes novel methods and compositions comprising asymmetric disulfides.
- the signals generated from label probes can be dependent on the behavior or properties of the SAM.
- SAMs comprising "nanoconduits” or “electroconduits”, as outlined in U.S.S.N. 60/145,912 hereby expressly incorporated herein by reference in its entirety, give good signals.
- the present invention provides asymmetric insulators based on disulfides, wherein one of the arms being a longer alkyl chain (or other SAM forming species) and the other arm comprising either a shorter alkyl chain or a bulky group, such as a branched alkyl group, that can be polar or nonpolar) for creating the nanoconduits.
- exemplary species and methods of making are described in U.S.S.N. 09/847,113. See also Mukaiyama Tetrahedron Lett. 1968, 5907; Boustany Tetrahedron Lett. 1970 3547; Harpp Tetrahedron Lett. 1970 3551; and Oae, J. Chem. Soc. Chem. Commun, 1977, 407, all of which are expressly incorporated herein by reference.
- the length of the species making up the monolayer will vary as needed. As outlined above, it appears that hybridization is more efficient at a distance from the surface.
- the species to which nucleic acids are attached (as outlined below, these can be either insulators or conductive oligomers) may be basically the same length as the monolayer forming species or longer than them, resulting in the nucleic acids being more accessible to the solvent for hybridization.
- the conductive oligomers to which the nucleic acids are attached may be shorter than the monolayer.
- the actual combinations and ratios of the different species making up the monolayer can vary widely, and will depend on whether mechanism-1 or -2 is used. Generally, either two or three component systems are preferred for mechanism-2 systems. Three component systems utilize a first species comprising a capture probe containing species, attached to the electrode via either an insulator or a conductive oligomer. The second species are conductive oligomers, and the third species are insulators.
- the first species can comprise from about 90% to about 1 %, with from about 20% to about 40% being preferred. For nucleic acids, from about 30% to about 40% is especially preferred for short oligonucleotide targets and from about 10% to about 20% is preferred for longer targets.
- the second species can comprise from about 1% to about 90%, with from about 20% to about 90% being preferred, and from about 40% to about 60% being especially preferred.
- the third species can comprise from about 1% to about 90%, with from about 20% to about 40% being preferred, and from about 15% to about 30% being especially preferred.
- preferred ratios of first:second:third species in SAM formation solvents are 2:2:1 for short targets, 1:3:1 for longer targets, with total thiol concentration (when used to attach these species, as is more fully outlined below) in the 500 ⁇ M to 1 mM range, and 833 ⁇ M being preferred.
- two component systems can be used.
- the two components are the first and second species.
- the first species can comprise from about 1% to about 90%, with from about 1% to about 40% being preferred, and from about 10% to about 40% being especially preferred.
- the second species can comprise from about 1% to about 90%, with from about 10% to about 60% being preferred, and from about 20% to about 40% being especially preferred.
- the two components are the first and the third species.
- the first species can comprise from about 1% to about 90%, with from about 1% to about 40% being preferred, and from about 10% to about 40% being especially preferred.
- the second species can comprise from about 1 % to about 90%, with from about 10% to about 60% being preferred, and from about 20% to about 40% being especially preferred.
- the deposition of the SAM is done using aqueous solvents.
- aqueous solvents As is generally described in Steel et al., Anal. Chem. 70:4670 (1998), Herne et al., J. Am. Chem. Soc. 119:8916 (1997), and Finklea, Electrochemistry of Organized Monolayers of Thiols and Related Molecules on Electrodes, from A.J. Bard, Electroanalvtical Chemistry: A Series of Advances. Vol. 20, Dekker N.Y. 1966-, all of which are expressly incorporated by reference, the deposition of the SAM-forming species can be done out of aqueous solutions, frequently comprising salt.
- the covalent attachment of the conductive oligomers and insulators may be accomplished in a variety of ways, depending on the electrode and the composition of the insulators and conductive oligomers used.
- the attachment linkers with covalently attached nucleosides or nucleic acids as depicted herein are covalently attached to an electrode.
- one end or terminus of the attachment linker is attached to the nucleoside or nucleic acid, and the other is attached to an electrode.
- attachment linker may be attached at two sites to the electrode, as is generally depicted in Structures 11-13.
- some type of linker is used, as depicted below as “A” in Structure 10, where "X” is the conductive oligomer, "I” is an insulator and the hatched surface is the electrode:
- A is a linker or atom.
- A may be a sulfur moiety when a gold electrode is used.
- A may be a silicon (silane) moiety attached to the oxygen of the oxide (see for example Chen et al., Langmuir 10:3332-3337 (1994); Lenhard et al., J. Electroanal. Chem. 78:195-201 (1977), both of which are expressly incorporated by reference).
- A may be an amino moiety (preferably a primary amine; see for example Deinhammer et al., Langmuir 10:1306-1313 (1994)).
- preferred A moieties include, but are not limited to, silane moieties, sulfur moieties (including alkyl sulfur moieties), and amino moieties.
- epoxide type linkages with redox polymers such as are known in the art are not used.
- the insulators and conductive oligomers may be attached to the electrode with more than one "A" moiety; the "A" moieties may be the same or different.
- the electrode is a gold electrode
- "A" is a sulfur atom or moiety
- multiple sulfur atoms may be used to attach the conductive oligomer to the electrode, such as is generally depicted below in Structures 11, 12 and 13.
- the A moiety is just a sulfur atom, but substituted sulfur moieties may also be used.
- a conductive oligomer terminating in a single carbon atom with three sulfur moities attached to the electrode may also comprise a "Q" terminal group.
- the electrode is a gold electrode, and attachment is via a sulfur linkage as is well known in the art, i.e. the A moiety is a sulfur atom or moiety. Although the exact characteristics of the gold-sulfur attachment are not known, this linkage is considered covalent for the purposes of this invention.
- a representative structure is depicted in Structure 14, using the Structure 3 conductive oligomer, although as for all the structures depicted herein, any of the conductive oligomers, or combinations of conductive oligomers, may be used. Similarly, any of the conductive oligomers or insulators may also comprise terminal groups as described herein.
- Structure 14 depicts the "A" linker as comprising just a sulfur atom, although additional atoms may be present (i.e. linkers from the sulfur to the conductive oligomer or substitution groups).
- Structure 14 shows the sulfur atom attached to the Y aromatic group, but as will be appreciated by those in the art, it may be attached to the B-D group (i.e. an acetylene) as well.
- the electrode is a carbon electrode, i.e. a glassy carbon electrode, and attachment is via a nitrogen of an amine group.
- a representative structure is depicted in Structure 15. Again, additional atoms may be present, i.e. Z type linkers and/or terminal groups.
- the oxygen atom is from the oxide of the metal oxide electrode.
- the Si atom may be combined with other atoms, i.e. be a silicon moiety containing substitution groups.
- Other attachments for SAMs to other electrodes are known in the art; see for example Napier et al., Langmuir, 1997, for attachment to indium tin oxide electrodes, and also the chemisorption of phosphates to an indium tin oxide electrode (talk by H. Holden Thorpe, CHI conference, May 4-5, 1998).
- the SAMs of the invention can be made in a variety of ways, including deposition out of organic solutions and deposition out of aqueous solutions.
- the methods outlined herein use a gold electrode as the example, although as will be appreciated by those in the art, other metals and methods may be used as well.
- ITO indium-tin-oxide
- a gold surface is first cleaned.
- cleaning procedures including, but not limited to, chemical cleaning or etchants including Piranha solution (hydrogen peroxide/sulfuric acid) or aqua regia (hydrochloric acid/nitric acid), electrochemical methods, flame treatment, plasma treatment or combinations thereof.
- the gold substrate is exposed to the SAM species.
- the SAM species are phosphonate-containing species.
- This can also be done in a variety of ways, including, but not limited to, solution deposition, gas phase deposition, microcontact printing, spray deposition, deposition using neat components, etc.
- a preferred embodiment utilizes a deposition solution comprising a mixture of various SAM species in solution, generally thiol-containing species. Mixed monolayers that contain nucleic acids are usually prepared using a two step procedure.
- the thiolated nucleic acid is deposited during the first deposition step (generally in the presence of at least one other monolayer-forming species) and the mixed monolayer formation is completed during the second step in which a second thiol solution minus nucleic acid is added.
- a second step utilizing mild heating to promote monolayer reorganization.
- the deposition solution is an organic deposition solution.
- a clean gold surface is placed into a clean vial.
- a binding ligand deposition solution in organic solvent is prepared in which the total thiol concentration is, between micromolar to saturation; preferred ranges include from about 1 ⁇ M to 10 mM, with from about 400 uM to about 1.0 mM being especially preferred.
- the deposition solution contains thiol modified DNA (i.e. nucleic acid attached to an attachment linker) and thiol diluent molecules (either conductive oligomers or insulators, with the latter being preferred).
- the ratio of nucleic acid to diluent is usually between 1000:1 to 1:1000, with from about 10:1 to about 1:10 being preferred and 1:1 being especially preferred.
- the preferred solvents are tetrahydrofuran (THF), acetonitrile, dimethylforamide (DMF), ethanol, or mixtures thereof; generally any solvent of sufficient polarity to dissolve the capture ligand can be used, as long as the solvent is devoid of functional groups that will react with the surface.
- Sufficient nucleic acid deposition solution is added to the vial so as to completely cover the electrode surface.
- the gold substrate is allowed to incubate at ambient temperature or slightly above ambient temperature for a period of time ranging from seconds to hours, with 5-30 minutes being preferred.
- the deposition solution is removed and a solution of diluent molecule only (from about 1 ⁇ M to 10 mM, with from about 100 uM to about 1.0 mM being preferred) in organic solvent is added.
- the gold substrate is allowed to incubate at room temperature or above room temperature for a period of time (seconds to days, with from about 10 minutes to about 24 hours being preferred).
- the gold sample is removed from the solution, rinsed in clean solvent and used.
- an aqueous deposition solution is used.
- a clean gold surface is placed into a clean vial.
- a nucleic acid deposition solution in water is prepared in which the total thiol concentration is between about 1 uM and 10 mM, with from about 1 ⁇ M to about 200 uM being preferred.
- the aqueous solution frequently has salt present (up to saturation, with approximately 1 being preferred), however pure water can be used.
- the deposition solution contains thiol modified nucleic acid and often a thiol diluent molecule.
- the ratio of nucleic acid to diluent is usually between 1000:1 to 1 :1000, with from about 10:1 to about 1 :10 being preferred and 1 :1 being especially preferred.
- the nucleic acid deposition solution is added to the vial in such a volume so as to completely cover the electrode surface.
- the gold substrate is allowed to incubate at ambient temperature or slightly above ambient temperature for 1-30 minutes with 5 minutes usually being sufficient. After the initial incubation, the deposition solution is removed and a solution of diluent molecule only (10 uM -1.0 mM) in either water or organic solvent is added.
- the gold substrate is allowed to incubate at room temperature or above room temperature until a complete monolayer is formed (10 minutes-24 hours). The gold sample is removed from the solution, rinsed in clean solvent and used.
- the deposition solution comprises a zwitterionic compound, preferably betaine.
- Preferred embodiments utilize betaine and Tris-HCI buffers.
- a circuit board is used as the substrate for the gold electrodes. Formation of the SAMs on the gold surface is generally done by first cleaning the boards, for example in a 10% sulfuric acid solution for 30 seconds, detergent solutions, aqua regia, plasma, etc., as outlined herein. Following the sulfuric acid treatment, the boards are washed, for example via immersion in two Milli-Q water baths for 1 minute each. The boards are then dried, for example under a stream of nitrogen. Spotting of the deposition solution onto the boards is done using any number of known spotting systems, generally by placing the boards on an X-Y table, preferably in a humidity chamber.
- the size of the spotting drop will vary with the size of the electrodes on the boards and the equipment used for delivery of the solution; for example, for 250 ⁇ M size electrodes, a 30 nanoliter drop is used. The volume should be sufficient to cover the electrode surface completely.
- the drop is incubated at room temperature for a period of time (sec to overnight, with 5 minutes preferred) and then the drop is removed by rinsing in a Milli-Q water bath.
- the boards are then optionally treated with a second deposition solution, generally comprising insulator in organic solvent, preferably acetonitrile, by immersion in a 45°C bath. After 30 minutes, the boards are removed and immersed in an acetonitrile bath for 30 seconds followed by a milli-Q water bath for 30 seconds.
- the boards are dried under a stream of nitrogen. Preferrably, only the water rinse is employed.
- the detection electrode comprising the SAM (or the sites on the array, for non-electrode embodiments) further comprises capture binding ligands, preferably covalently attached.
- binding ligand or “binding species” herein is meant a compound that is used to probe for the presence of the target analyte, that will bind to the target analyte.
- binding ligands used per target analyte molecule; a “capture” or “anchor” binding ligand (also referred to herein as a “capture probe”, particularly in reference to a nucleic acid binding ligand) that is attached to the detection electrode as described herein, and a soluble binding ligand (frequently referred to herein as a “signaling probe” or a “label probe”), that binds independently to the target analyte, and either directly or indirectly comprises at least one ETM.
- a “capture” or “anchor” binding ligand also referred to herein as a “capture probe”, particularly in reference to a nucleic acid binding ligand
- a soluble binding ligand frequently referred to herein as a “signaling probe” or a “label probe”
- the target sequence is generally amplified, and during amplification, a fluorescent label is added; thus these systems generally comprise only two elements, the capture probe and the labeled target.
- the discussion below is directed to the use of electrodes and electrochemical detection, but as will be appreciated by those in the art, fluorescent based systems can be used as well.
- the capture binding ligand allows the attachment of a target analyte to the detection electrode, for the purposes of detection.
- attachment of the target analyte to the capture binding ligand may be direct (i.e. the target analyte binds to the capture binding ligand) or indirect (one or more capture extender ligands may be used).
- the binding is specific, and the binding ligand is part of a binding pair.
- specifically bind herein is meant that the ligand binds the analyte, with specificity sufficient to differentiate between the analyte and other components or contaminants of the test sample.
- the systems may use different binding ligands, for example an array of different ligands, and detection of any particular analyte is via its "signature" of binding to a panel of binding ligands, similar to the manner in which "electronic noses" work.
- the binding should be sufficient to allow the analyte to remain bound under the conditions of the assay, including wash steps to remove non-specific binding.
- the binding constants of the analyte to the binding ligand will be at least about 10 "4 to 10 " 9 M " ⁇ with at least about 10 "5 to 10 "9 being preferred and at least about 10 "7 to 10 "9 M "1 being particularly preferred.
- the composition of the binding ligand will depend on the composition of the target analyte. Binding ligands to a wide variety of analytes are known or can be readily found using known techniques. For example, when the analyte is a single-stranded nucleic acid, the binding ligand is generally a substantially complementary nucleic acid. Alternatively, as is generally described in U.S. Patents 5,270,163, 5,475,096, 5,567,588, 5,595,877, 5,637,459, 5,683,867, 5,705,337, and related patents, hereby incorporated by reference, nucleic acid "aptamers" can be developed for binding to virtually any target analyte.
- the analyte may be a nucleic acid binding protein and the capture binding ligand is either a single-stranded or double-stranded nucleic acid; alternatively, the binding ligand may be a nucleic acid binding protein when the analyte is a single or double-stranded nucleic acid.
- the binding ligands include proteins (particularly including antibodies or fragments thereof (FAbs, etc.)), small molecules, or aptamers, described above.
- Preferred binding ligand proteins include peptides.
- suitable binding ligands include substrates, inhibitors, and other proteins that bind the enzyme, i.e.
- any two molecules that will associate, preferably specifically, may be used, either as the analyte or the binding ligand.
- Suitable analyte/binding ligand pairs include, but are not limited to, antibodies/antigens, receptors/ligand, proteins/nucleic acids; nucleic acids/nucleic acids, enzymes/substrates and/or inhibitors, carbohydrates (including glycoproteins and glycolipids)/lectins, carbohydrates and other binding partners, proteins/proteins; and protein/small molecules. These may be wild-type or derivative sequences.
- the binding ligands are portions (particularly the extracellular portions) of cell surface receptors that are known to multimerize, such as the growth hormone receptor, glucose transporters (particularly GLUT4 receptor), transferrin receptor, epidermal growth factor receptor, low density lipoprotein receptor, high density lipoprotein receptor, leptin receptor, interleukin receptors including IL-1 , IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-11, IL- 12, IL-13, IL-15 and IL-17 receptors, VEGF receptor, PDGF receptor, EPO receptor, TPO receptor, ciliary neurotrophic factor receptor, prolactin receptor, and T-cell receptors.
- cell surface receptors such as the growth hormone receptor, glucose transporters (particularly GLUT4 receptor), transferrin receptor, epidermal growth factor receptor, low density lipoprotein receptor, high density lipoprotein receptor, leptin receptor, interleukin receptors including IL-1 , IL
- the binding ligand is a nucleic acid
- preferred compositions and techniques are outlined in U.S. Patent Nos. 5,591,578; 5,824,473; 5,705,348; 5,780,234 and 5,770,369; U.S.S.N.s 08/873,598 08/911,589; WO 98/20162; WO98/12430; W098/57158; WO 00/16089) W099/57317; W099/67425; WO00/24941; PCT USOO/10903; WO00/38836; W099/37819; W099/57319 and PCTUS00/20476; and related materials, all of which are expressly incorporated by reference in their entirety.
- the method of attachment of the capture binding ligands to the attachment linker will generally be done as is known in the art, and will depend on both the composition of the attachment linker and the capture binding ligand.
- the capture binding ligands are attached to the attachment linker through the use of functional groups on each that can then be used for attachment.
- Preferred functional groups for attachment are amino groups, carboxy groups, oxo groups and thiol groups. These functional groups can then be attached, either directly or indirectly through the use of a linker, sometimes depicted herein as "Z".
- Linkers are well known in the art; for example, homo-or hetero-bifunctional linkers as are well known (see 1994 Pierce Chemical Company catalog, technical section on cross-linkers, pages 155-200, incorporated herein by reference).
- Preferred Z linkers include, but are not limited to, alkyl groups (including substituted alkyl groups and alkyl groups containing heteroatom moieties), with short alkyl groups, esters, amide, amine, epoxy groups and ethylene glycol and derivatives being preferred, with propyl, acetylene, and C 2 alkene being especially preferred.
- Z may also be a sulfone group, forming sulfonamide linkages.
- capture binding ligands comprising proteins, lectins, nucleic acids, small organic molecules, carbohydrates, etc. can be added.
- a preferred embodiment utilizes proteinaceous capture binding ligands.
- any number of techniques may be used to attach a proteinaceous capture binding ligand to an attachment linker.
- a wide variety of techniques are known to add moieties to proteins.
- a preferred embodiment utilizes nucleic acids as the capture binding ligand. While most of the following discussion focuses on nucleic acids, as will be appreciated by those in the art, many of the techniques outlined below apply in a similar manner to non-nucleic acid systems as well, and to systems that rely on attachment to surfaces other than metal electrodes.
- the capture probe nucleic acid is covalently attached to the electrode, via an “attachment linker”, that can be either a conductive oligomer (required for mechanism-1 systems) or an insulator.
- an “attachment linker” can be either a conductive oligomer (required for mechanism-1 systems) or an insulator.
- covalently attached herein is meant that two moieties are attached by at least one bond, including sigma bonds, pi bonds and coordination bonds.
- nucleic acid or other binding ligand
- the other end is attached to the electrode.
- any of the structures depicted herein may further comprise a nucleic acid effectively as a terminal group.
- the present invention provides compositions comprising nucleic acids covalently attached to electrodes as is generally depicted below in Structure 17:
- X is a conductive oligomer and I is an insulator as defined herein.
- F. is a linkage that allows the covalent attachment of the electrode and the conductive oligomer or insulator, including bonds, atoms or linkers such as is described herein, for example as "A", defined below.
- F 2 is a linkage that allows the covalent attachment of the conductive oligomer or insulator to the nucleic acid, and may be a bond, an atom or a linkage as is herein described.
- F 2 may be part of the conductive oligomer, part of the insulator, part of the nucleic acid, or exogeneous to both, for example, as defined herein for "Z".
- the capture probe nucleic acid is covalently attached to the electrode via an attachment linker.
- the covalent attachment of the nucleic acid and the attachment linker may be accomplished in several ways.
- the attachment is via attachment to the base of the nucleoside, via attachment to the backbone of the nucleic acid (either the ribose, the phosphate, or to an analogous group of a nucleic acid analog backbone), or via a transition metal ligand, as described below.
- the techniques outlined below are generally described for naturally occurring nucleic acids, although as will be appreciated by those in the art, similar techniques may be used with nucleic acid analogs, and in some cases with other binding ligands.
- most of the structures herein depict conductive oligomers as the attachment linkers, but insulators such as alkyl chains are preferred in many embodiments.
- the attachment linker is attached to the base of a nucleoside of the nucleic acid. This may be done in several ways, depending on the linker, as is described below. In one embodiment, the linker is attached to a terminal nucleoside, i.e. either the 3' or 5' nucleoside of the nucleic acid. Alternatively, the linker is attached to an internal nucleoside.
- the point of attachment to the base will vary with the base. Generally, attachment at any position is possible. In some embodiments, for example when the probe containing the ETMs may be used for hybridization (i.e. mechanism-1 systems) , it is preferred to attach at positions not involved in hydrogen bonding to the complementary base. Thus, for example, generally attachment is to the 5 or 6 position of pyrimidines such as uridine, cytosine and thymine. For purines such as adenine and guanine, the linkage is preferably via the 8 position. Attachment to non-standard bases is preferably done at the comparable positions.
- the attachment is direct; that is, there are no intervening atoms between the attachment linker and the base.
- attachment linkers comprising conductive oligomers with terminal acetylene bonds are attached directly to the base.
- Structure 18 is an example of this linkage, using a Structure 3 conductive oligomer and uridine as the base, although other bases and attachment linkers can be used as will be appreciated by those in the art:
- the pentose structures depicted herein may have hydrogen, hydroxy, phosphates or other groups such as amino groups attached.
- the pentose and nucleoside structures depicted herein are depicted non-conventionally, as mirror images of the normal rendering.
- the pentose and nucleoside structures may also contain additional groups, such as protecting groups, at any position, for example as needed during synthesis.
- the base may contain additional modifications as needed, i.e. the carbonyl or amine groups may be altered or protected.
- the attachment is any number of different Z linkers, including amide and amine linkages, as is generally depicted in Structure 19 using uridine as the base and a Structure 3 oligomer as the attachment linker:
- Z is a linker.
- Z is a short linker of about 1 to about 10 atoms, with from 1 to 5 atoms being preferred, that may or may not contain alkene, alkynyl, amine, amide, azo, imine, etc., bonds.
- Linkers are known in the art; for example, homo-or hetero-bifunctional linkers as are well known (see 1994 Pierce Chemical Company catalog, technical section on cross-linkers, pages 155-200, incorporated herein by reference).
- Preferred Z linkers include, but are not limited to, alkyl groups (including substituted alkyl groups and alkyl groups containing heteroatom moieties), with short alkyl groups, esters, amide, amine, epoxy groups and ethylene glycol and derivatives being preferred, with propyl, acetylene, and C 2 alkene being especially preferred.
- Z may also be a sulfone group, forming sulfonamide linkages as discussed below.
- the attachment of the nucleic acid and the attachment linker is done via attachment to the backbone of the nucleic acid. This may be done in a number of ways, including attachment to a ribose of the ribose-phosphate backbone, or to the phosphate of the backbone, or other groups of analogous backbones.
- the site of attachment in this embodiment may be to a 3' or 5' terminal nucleotide, or to an internal nucleotide, as is more fully described below.
- the attachment linker is attached to the ribose of the ribose-phosphate backbone.
- nucleosides that are modified at either the 2' or 3' position of the ribose with amino groups, sulfur groups, silicone groups, phosphorus groups, or oxo groups can be made (Imazawa et al., J. Org. Chem., 44:2039 (1979); Hobbs et al., J. Org. Chem. 42(4):714 (1977); Verheyden et al., J. Orrg. Chem. 36(2):250 (1971); McGee et al., J. Org. Chem.
- a preferred embodiment utilizes amino-modified nucleosides. These amino-modified riboses can then be used to form either amide or amine linkages to the conductive oligomers.
- the amino group is attached directly to the ribose, although as will be appreciated by those in the art, short linkers such as those described herein for "Z" may be present between the amino group and the ribose.
- an amide linkage is used for attachment to the ribose.
- m is zero and thus the conductive oligomer terminates in the amide bond.
- the nitrogen of the amino group of the amino-modified ribose is the "D" atom of the conductive oligomer.
- Structure 20 has the terminal bond fixed as an amide bond.
- a heteroatom linkage is used, i.e. oxo, amine, sulfur, etc.
- a preferred embodiment utilizes an amine linkage.
- the nitrogen of the amino-modified ribose may be the "D" atom of the conductive oligomer when the Structure 3 conductive oligomer is used.
- Structures 21 and 22 depict nucleosides with the Structures 3 and 9 conductive oligomers, respectively, as the attachment linkers, using the nitrogen as the heteroatom, athough other heteroatoms can be used:
- both m and t are not zero.
- a preferred Z here is a methylene group, or other aliphatic alkyl linkers. One, two or three carbons in this position are particularly useful for synthetic reasons.
- Z is as defined above.
- Suitable linkers include methylene and ethylene.
- the attachment linker is covalently attached to the nucleic acid via the phosphate of the ribose-phosphate backbone (or analog) of a nucleic acid.
- the attachment is direct, utilizes a linker or via an amide bond.
- Structure 23 depicts a direct linkage
- Structure 24 depicts linkage via an amide bond (both utilize the Structure 3 conductive oligomer, although Structure 8 conductive oligomers are also possible as well as any number of other attachment linkers).
- Structures 23 and 24 depict the conductive oligomer in the 3' position, although the 5' position is also possible.
- both Structures 23 and 24 depict naturally occurring phosphodiester bonds, although as those in the art will appreciate, non-standard analogs of phosphodiester bonds may also be used.
- Structure 24 depicts a preferred embodiment, wherein the terminal B-D bond is an amide bond, the terminal Y is not present, and Z is a linker, as defined herein.
- the attachment linker is covalently attached to the nucleic acid via a transition metal ligand.
- the attachment linker is covalently attached to a ligand which provides one or more of the coordination atoms for a transition metal.
- the ligand to which the attachment linker is attached also has the nucleic acid attached, as is generally depicted below in Structure 25.
- the attachment linker is attached to one ligand, and the nucleic acid is attached to another ligand, as is generally depicted below in Structure 26.
- the attachment linker is covalently attached to the nucleic acid. Both of these structures depict Structure 3 conductive oligomers, although other attachment linkers may be utilized. Structures 25 and 26 depict two representative structures:
- M is a metal atom, with transition metals being preferred.
- Suitable transition metals for use in the invention include, but are not limited to, cadmium (Cd), copper (Cu), cobalt (Co), palladium (Pd), zinc (Zn), iron (Fe), ruthenium (Ru), rhodium (Rh), osmium (Os), rhenium (Re), platinium (Pt), scandium (Sc), titanium (Ti), Vanadium (V), chromium (Cr), manganese (Mn), nickel (Ni), Molybdenum (Mo), technetium (Tc), tungsten (W), and iridium (Ir).
- the first series of transition metals the platinum metals (Ru, Rh, Pd, Os, Ir and Pt), along with Fe, Re, W, Mo and Tc, are preferred.
- Particularly preferred are ruthenium, rhenium, osmium, platinium, cobalt and iron.
- L are the co-ligands, that provide the coordination atoms for the binding of the metal ion.
- the number and nature of the co-ligands will depend on the coordination number of the metal ion.
- Mono-, di- or polydentate co-ligands may be used at any position.
- r may range from zero (when all coordination atoms are provided by the other two ligands) to four, when all the co-ligands are monodentate.
- r will be from 0 to 8, depending on the coordination number of the metal ion and the choice of the other ligands.
- the metal ion has a coordination number of six and both the ligand attached to the conductive oligomer and the ligand attached to the nucleic acid are at least bidentate; that is, r is preferably zero, one (i.e. the remaining co-ligand is bidentate) or two (two monodentate co-ligands are used).
- the co-ligands can be the same or different. Suitable ligands fall into two categories: ligands which use nitrogen, oxygen, sulfur, carbon or phosphorus atoms (depending on the metal ion) as the coordination atoms (generally referred to in the literature as sigma ( ⁇ ) donors) and organometallic ligands such as metallocene ligands (generally referred to in the literature as pi ( ⁇ ) donors, and depicted herein as LJ.
- Suitable nitrogen donating ligands are well known in the art and include, but are not limited to, NH 2 ; NHR; NRR'; pyridine; pyrazine; isonicotinamide; imidazole; bipyridine and substituted derivatives of bipyridine; terpyridine and substituted derivatives; phenanthrolines, particularly 1 ,10-phenanthroline (abbreviated phen) and substituted derivatives of phenanthrolines such as 4,7-dimethylphenanthroline and dipyridol[3,2-a:2',3'-c]phenazine (abbreviated dppz); dipyridophenazine; 1 ,4,5,8,9,12-hexaazatriphenylene (abbreviated hat); 9,10- phenanthrenequinone diimine (abbreviated phi); 1,4,5,8-tetraazaphenanthrene (abbreviated tap); 1,4,8,11-tetra-azacyclotetradecan
- Substituted derivatives including fused derivatives, may also be used.
- porphyrins and substituted derivatives of the porphyrin family may be used. See for example, Comprehensive Coordination Chemistry, Ed. Wilkinson et al., Pergammon Press, 1987, Chapters 13.2 (pp73-98), 21.1 (pp. 813-898) and 21.3 (pp 915-957), all of which are hereby expressly incorporated by reference.
- Suitable sigma donating ligands using carbon, oxygen, sulfur and phosphorus are known in the art.
- suitable sigma carbon donors are found in Cotton and Wilkenson, Advanced Organic Chemistry, 5th Edition, John Wiley & Sons, 1988, hereby incorporated by reference; see page 38, for example.
- suitable oxygen ligands include crown ethers, water and others known in the art.
- Phosphines and substituted phosphines are also suitable; see page 38 of Cotton and Wilkenson.
- oxygen, sulfur, phosphorus and nitrogen-donating ligands are attached in such a manner as to allow the heteroatoms to serve as coordination atoms.
- organometallic ligands are used.
- transition metal organometallic compounds with ⁇ -bonded organic ligands see Advanced Inorganic Chemistry, 5th Ed., Cotton & Wilkinson, John Wiley & Sons, 1988, chapter 26; Organometallics, A Concise Introduction, Elschenbroich et al., 2nd Ed., 1992, VCH; and Comprehensive Organometallic Chemistry II, A Review of the Literature 1982-1994, Abel et al. Ed., Vol.
- organometallic ligands include cyclic aromatic compounds such as the cyclopentadienide ion [C 5 H 5 (-1)] and various ring substituted and ring fused derivatives, such as the indenylide (-1) ion, that yield a class of bis(cyclopentadieyl) metal compounds, (i.e. the metallocenes); see for example Robins et al., J. Am. Chem. Soc. 104:1882-1893 (1982); and Gassman et al., J. Am. Chem. Soc. 108:4228-4229 (1986), incorporated by reference.
- cyclic aromatic compounds such as the cyclopentadienide ion [C 5 H 5 (-1)]
- various ring substituted and ring fused derivatives such as the indenylide (-1) ion
- ferrocene [(C 5 H 5 ) 2 Fej and its derivatives are prototypical examples which have been used in a wide variety of chemical (Connelly et al., Chem. Rev. 96:877- 910 (1996), incorporated by reference) and electrochemical (Geiger et al., Advances in Organometallic Chemistry 23:1-93; and Geiger et al., Advances in Organometallic Chemistry 24:87, incorporated by reference) electron transfer or "redox" reactions.
- Metallocene derivatives of a variety of the first, second and third row transition metals are potential candidates as redox moieties that are covalently attached to either the ribose ring or the nucleoside base of nucleic acid.
- organometallic ligands include cyclic arenes such as benzene, to yield bis(arene)metal compounds and their ring substituted and ring fused derivatives, of which bis(benzene)chromium is a prototypical example
- Other acyclic ⁇ -bonded ligands such as the allyl(-1) ion, or butadiene yield potentially suitable organometallic compounds, and all such ligands, in conjuction with other ⁇ -bonded and o-bonded ligands constitute the general class of organometallic compounds in which there is a metal to carbon bond. Electrochemical studies of various dimers and oligomers of such compounds with bridging organic ligands, and additional non-bridging ligands, as well as with and without metal- metal bonds are potential candidate redox moieties in nucleic acid analysis.
- the ligand is generally attached via one of the carbon atoms of the organometallic ligand, although attachment may be via other atoms for heterocyclic ligands.
- Preferred organometallic ligands include metallocene ligands, including substituted derivatives and the metalloceneophanes (see page 1174 of Cotton and Wilkenson, supra).
- derivatives of metallocene ligands such as methylcyclopentadienyl, with multiple methyl groups being preferred, such as pentamethylcyclopentadienyl, can be used to increase the stability of the metallocene.
- only one of the two metallocene ligands of a metallocene are derivatized.
- any combination of ligands may be used.
- Preferred combinations include: a) all ligands are nitrogen donating ligands; b) all ligands are organometallic ligands; and c) the ligand at the terminus of the attachment linker is a metallocene ligand and the ligand provided by the nucleic acid is a nitrogen donating ligand, with the other ligands, if needed, are either nitrogen donating ligands or metallocene ligands, or a mixture.
- attachment linkers such as alkyl groups may also be utilized.
- the ligands used in the invention show altered fluorescent properties depending on the redox state of the chelated metal ion. As described below, this thus serves as an additional mode of detection of electron transfer between the ETM and the electrode.
- the ligand attached to the nucleic acid is an amino group attached to the 2' or 3' position of a ribose of the ribose-phosphate backbone.
- This ligand may contain a multiplicity of amino groups so as to form a polydentate ligand which binds the metal ion.
- Other preferred ligands include cyclopentadiene and phenanthroline.
- the capture probe nucleic acids are covalently attached to the electrode via an insulator (i.e. the attachment linker is an insulator).
- an insulator i.e. the attachment linker is an insulator.
- the attachment of nucleic acids (and other binding ligands) to insulators such as alkyl groups is well known, and can be done to the base or the backbone, including the ribose or phosphate for backbones containing these moieties, or to alternate backbones for nucleic acid analogs.
- different capture probes, or one capture probe with a multiplicity of different capture extender probes can be used.
- a number of capture probes are designed and used for each target sequence. That is, a single electrode pad of the array may have 1 probe to the target analyte, or a plurality of probes to the same target sequence, preferably (but not required to be) non-overlapping. This is particularly preferred for long target sequences. In this embodiment, at least two different capture probes are used, with at least 3, 4, 5, 6, 7, 8, 9 or 10 being preferred, and 8 being particularly preferred.
- the present invention provides substrates comprising at least one detection electrode comprising monolayers and capture binding ligands, useful in target analyte detection systems.
- the compositions further comprise a solution or soluble binding ligand, although as is more fully described below, for mechanism-1 systems, the ETMs may be added in the form of non-covalently attached hybridization indicators.
- Solution binding ligands are similar to capture binding ligands, in that they bind, preferably specifically, to target analytes.
- the solution binding ligand (generally referred to herein as label probes when the target analytes are nucleic acids) may be the same or different from the capture binding ligand. Generally, the solution binding ligands are not directly attached to the surface.
- the solution binding ligand either directly comprises a recruitment linker that comprises at least one ETM ( Figure 4A from 60/190,259), or the recruitment linker binds, either directly (Figure 4A) or indirectly (Figure 4E), to the solution binding ligand.
- solution binding ligands or “soluble binding ligands” or “signal carriers” or “label probes” or “label binding ligands” with recruitment linkers comprising covalently attached ETMs are provided. That is, one portion of the label probe or solution binding ligand directly or indirectly binds to the target analyte, and one portion comprises a recruitment linker comprising covalently attached ETMs. In some systems, for example in mechanism-1 nucleic acid systems, these may be the same. Similarly, for mechanism-1 systems, the recruitment linker comprises nucleic acid that will hybridize to detection probes.
- ETMs electron donor moiety
- ETMs electron acceptor moiety
- ETMs electron acceptor moiety
- ETMs electron acceptor moiety
- grammatical equivalents herein refers to molecules capable of electron transfer under certain conditions. It is to be understood that electron donor and acceptor capabilities are relative; that is, a molecule which can lose an electron under certain experimental conditions will be able to accept an electron under different experimental conditions. It is to be understood that the number of possible electron donor moieties and electron acceptor moieties is very large, and that one skilled in the art of electron transfer compounds will be able to utilize a number of compounds in the present invention.
- Preferred ETMs include, but are not limited to, transition metal complexes, organic ETMs, and electrodes.
- the ETMs are transition metal complexes.
- Transition metals are those whose atoms have a partial or complete d shell of electrons. Suitable transition metals for use in the invention are listed above.
- the transition metals are complexed with a variety of ligands, L, defined above, to form suitable transition metal complexes, as is well known in the art.
- Preferred ETMs comprise metallocenes, particularly ferrocene.
- organic electron donors and acceptors may be covalently attached to the nucleic acid for use in the invention.
- organic molecules include, but are not limited to, riboflavin, xanthene dyes, azine dyes, acridine orange, ⁇ /,/V-dimethyl-2J- diazapyrenium dichloride (DAP 2+ ), methylviologen, ethidium bromide, quinones such as N,N'- dimethylanthra(2,1,9-def.6,5,10-cf'e'f)diisoquinoline dichloride (ADIQ 2+ ); porphyrins ([meso-tetrakis(N- methyl-x-pyridinium)porphyrin tetrachloride], varlamine blue B hydrochloride, Bindschedler's green; 2,6-dichloroindophenol, 2,6-dibromophenolindophenol; Brilliant crest
- the electron donors and acceptors are redox proteins as are known in the art. However, redox proteins in many embodiments are not preferred.
- ETMs The choice of the specific ETMs will be influenced by the type of electron transfer detection used, as is generally outlined below.
- Preferred ETMs are metallocenes, with ferrocene being particularly preferred.
- the present invention provides methods and compositions useful in the detection of nucleic acids and other target analytes.
- the compositions of the invention can take on a wide variety of configurations.
- preferred systems of the invention work as follows.
- a target nucleic acid sequence is attached (via hybridization) to an electrode comprising a monolayer, generally including conductive oligomers. This attachment can be either directly to a capture probe on the surface, or indirectly, using capture extender probes.
- the target sequence itself comprises the ETMs.
- a label probe is then added, forming an assay complex.
- the attachment of the label probe may be direct (i.e.
- the hybridization to a portion of the target sequence or indirect (i.e. hybridization to an amplifier probe that hybridizes to the target sequence), with all the required nucleic acids forming an assay complex.
- the second portion of the label probe, the "recruitment linker", containing the ETMs is brought into spatial proximity to the SAM surface on the electrode, and the presence of the ETM can then be detected electronically.
- the present invention provides electrodes comprising monolayers comprising SAM forming species and capture probes, useful in nucleic acid (or other target analyte) detection systems.
- the compositions further comprise a label probe.
- the label probe is nucleic acid, generally single stranded, although as more fully outlined below, it may contain double-stranded portions, ln mechanism-2 systems, the label probe comprises a first portion that is capable of hybridizing to a component of the assay complex, defined below, and a second portion that does not hybridize to a component of an assay complex and comprises at least one covalently attached ETM.
- hydrophobic ETMs are preferred in mechanism-2 systems; however, transition metal complexes, although charged, with one or more hydrophobic ligands, such as Ru and Os complexes, also give rise to good signals.
- hydrophobic ligands such as Ru and Os complexes
- electron transfer between the ETM and the electrode is facilitated by the use of linkers or spacers that allow the ETM some flexibility to penetrate into the monolayer; thus the N6 compositions of the invention have a four carbon linker attaching the ETM to the nucleic acid.
- a plurality of ETMs are used.
- the use of multiple ETMs provides signal amplification and thus allows more sensitive detection limits.
- the use of multiple ETMs on nucleic acids that hybridize to complementary strands can cause decreases in T m s of the hybridization complexes depending on the number, site of attachment and spacing between the multiple ETMs, this is not a factor when the ETMs are on the recruitment linker, since this does not hybridize to a complementary sequence.
- pluralities of ETMs are preferred, with at least about 2 ETMs per recruitment linker being preferred, and at least about 10 being particularly preferred, and at least about 20 to 50 being especially preferred. In some instances, very large numbers of ETMs (100 to 1000) can be used.
- the portion of the label probe (or target, in some embodiments) that comprises the ETMs can be nucleic acid, or it can be a non-nucleic acid linker that links the first hybridizable portion of the label probe to the ETMs. That is, since this portion of the label probe is not required for hybridization, it need not be nucleic acid, although this may be done for ease of synthesis.
- the recruitment linker may comprise double-stranded portions.
- the recruitment linker is nucleic acid (including analogs), and attachment of the ETMs can be via (1) a base; (2) the backbone, including the ribose, the phosphate, or comparable structures in nucleic acid analogs; (3) nucleoside replacement, described below; or (4) metallocene polymers, as described below.
- the recruitment linker is non-nucleic acid, and can be either a metallocene polymer or an alkyl-type polymer (including heteroalkyl, as is more fully described below) containing ETM substitution groups. These options are generally depicted in the Figures.
- the recruitment linker is a nucleic acid, and comprises covalently attached ETMs.
- the ETMs may be attached to nucleosides within the nucleic acid in a variety of positions. Preferred embodiments include, but are not limited to, (1) attachment to the base of the nucleoside, (2) attachment of the ETM as a base replacement, (3) attachment to the backbone of the nucleic acid, including either to a ribose of the ribose-phosphate backbone or to a phosphate moiety, or to analogous structures in nucleic acid analogs, and (4) attachment via metallocene polymers, with the latter being preferred.
- the recruitment linker is nucleic acid
- secondary label probes that have a first portion that will hybridize to a portion of the primary label probes and a second portion comprising a recruitment linker as is defined herein. This is generally depicted in Figure 16H of U.S.S.N. 60/190,259.
- the ETM is attached to the base of a nucleoside as is generally outlined above for attachment of the attachment linkers. Attachment can be to an internal nucleoside or a terminal nucleoside.
- the covalent attachment to the base will depend in part on the ETM chosen, but in general is similar to the attachment of conductive oligomers to bases, as outlined above. Attachment may generally be done to any position of the base.
- the ETM is a transition metal complex, and thus attachment of a suitable metal ligand to the base leads to the covalent attachment of the ETM.
- similar types of linkages may be used for the attachment of organic ETMs, as will be appreciated by those in the art.
- the C4 attached amino group of cytosine, the C6 attached amino group of adenine, or the C2 attached amino group of guanine may be used as a transition metal ligand.
- Ligands containing aromatic groups can be attached via acetylene linkages as is known in the art (see Comprehensive Organic Synthesis, Trost et al., Ed., Pergamon Press, Chapter 2.4: Coupling Reactions Between sp 2 and sp Carbon Centers, Sonogashira, pp521-549, and pp950-953, hereby incorporated by reference).
- Structure 30 depicts a representative structure in the presence of the metal ion and any other necessary ligands;, Structure 30 depicts uridine, although as for all the structures herein, any other base may also be used.
- L a is a ligand, which may include nitrogen, oxygen, sulfur or phosphorus donating ligands or organometallic ligands such as metallocene ligands.
- Suitable L a ligands include, but are not limited to, phenanthroline, imidazole, bpy and terpy.
- L r and M are as defined above. Again, it will be appreciated by those in the art, that a linker (“Z”) may be included between the nucleoside and the ETM.
- the linkage may be done using a linker, which may utilize an amide linkage (see generally Telser et al., J. Am. Chem. Soc. 111:7221-7226 (1989); Telser et al., J. Am. Chem. Soc. 111:7226-7232 (1989), both of which are expressly incorporated by reference).
- a linker which may utilize an amide linkage (see generally Telser et al., J. Am. Chem. Soc. 111:7221-7226 (1989); Telser et al., J. Am. Chem. Soc. 111:7226-7232 (1989), both of which are expressly incorporated by reference).
- amide linkage see generally Telser et al., J. Am. Chem. Soc. 111:7221-7226 (1989); Telser et al., J. Am. Chem. Soc. 111:7226-7232 (1989), both of which are expressly
- L is a ligand as defined above, with L r and M as defined above as well.
- L is amino, phen, byp and terpy.
- the ETM attached to a nucleoside is a metallocene; i.e. the L and L r of Structure 31 are both metallocene ligands, L m , as described above.
- Structure 32 depicts a preferred embodiment wherein the metallocene is ferrocene, and the base is uridine, although other bases may be used:
- Preferred metallocenes include ferrocene, cobaltocene and osmiumocene.
- the ETM is attached to a ribose at any position of the ribose-phosphate backbone of the nucleic acid, i.e. either the 5' or 3' terminus or any internal nucleoside.
- Ribose in this case can include ribose analogs.
- nucleosides that are modified at either the 2' or 3' position of the ribose can be made, with nitrogen, oxygen, sulfur and phosphorus-containing modifications possible. Amino-modified and oxygen-modified ribose is preferred. See generally PCT publication WO 95/15971 , incorporated herein by reference.
- modification groups may be used as a transition metal ligand, or as a chemically functional moiety for attachment of other transition metal ligands and organometallic ligands, or organic electron donor moieties as will be appreciated by those in the art.
- a linker such as depicted herein for "Z” may be used as well, or a conductive oligomer between the ribose and the ETM.
- Preferred embodiments utilize attachment at the 2' or 3' position of the ribose, with the 2' position being preferred.
- the conductive oligomers depicted in Structure 13, 14 and 15 may be replaced by ETMs; alternatively, the ETMs may be added to the free terminus of the conductive oligomer.
- a metallocene serves as the ETM, and is attached via an amide bond as depicted below in Structure 33.
- the examples outline the synthesis of a preferred compound when the metallocene is ferrocene.
- amine linkages are used, as is generally depicted in Structure 34.
- Z is a linker, as defined herein, with 1-16 atoms being preferred, and 2-4 atoms being particularly preferred, and t is either one or zero.
- oxo linkages are used, as is generally depicted in Structure 35.
- Z is a linker, as defined herein, and t is either one or zero.
- an ETM is attached to a phosphate at any position of the ribose-phosphate backbone of the nucleic acid. This may be done in a variety of ways.
- phosphodiester bond analogs such as phosphoramide or phosphoramidite linkages may be incorporated into a nucleic acid, where the heteroatom (i.e. nitrogen) serves as a transition metal ligand (see PCT publication WO 95/15971, incorporated by reference).
- the conductive oligomers depicted in Structures 23 and 24 may be replaced by ETMs.
- the composition has the structure shown in Structure 36.
- the ETM is attached via a phosphate linkage, generally through the use of a linker, Z.
- alkyl-based linkers can be used to create multiple branching structures comprising one or more ETMs at the terminus of each branch (although internal ETMs can be used as well). Generally, this is done by creating branch points containing multiple hydroxy groups, which optionally can then be used to add additional branch points. The terminal hydroxy groups can then be used in phosphoramidite reactions to add ETMs, as is generally done below for the nucleoside replacement and metallocene polymer reactions.
- the branch point can be an internal one or a terminal one, and can be a chemical branch point or a nucleoside branch point.
- an ETM such as a metallocene is used as a "nucleoside replacement", serving as an ETM.
- the distance between the two cyclopentadiene rings of ferrocene is similar to the orthongonal distance between two bases in a double stranded nucleic acid.
- Other metallocenes in addition to ferrocene may be used, for example, air stable metallocenes such as those containing cobalt or ruthenium.
- metallocene moieties may be incorporated into the backbone of a nucleic acid, as is generally depicted in Structure 37 (nucleic acid with a ribose-phosphate backbone) and Structure 38 (peptide nucleic acid backbone).
- Structures 37 and 38 depict ferrocene, although as will be appreciated by those in the art, other metallocenes may be used as well. In general, air stable metallocenes are preferred, including metallocenes utilizing ruthenium and cobalt as the metal. Structure 37
- Z is a linker as defined above, with generally short, alkyl groups, including heteroatoms such as oxygen being preferred. Generally, what is important is the length of the linker, such that minimal perturbations of a double stranded nucleic acid is effected, as is more fully described below. Thus, methylene, ethylene, ethylene glycols, propylene and butylene are all preferred, with ethylene and ethylene glycol being particularly preferred.
- each Z linker may be the same or different.
- Structure 37 depicts a ribose-phosphate backbone, although as will be appreciated by those in the art, nucleic acid analogs may also be used, including ribose analogs and phosphate bond analogs.
- ETMs in addition to metallocenes, as nucleoside replacements or in polymer embodiments, described below.
- the ETM is a transition metal complex other than a metallocene, comprising one, two or three (or more) ligands
- the ligands can be functionalized as depicted for the ferrocene to allow the addition of phosphoramidite groups.
- Particularly preferred in this embodiment are complexes comprising at least two ring (for example, aryl and substituted aryl) ligands, where each of the ligands comprises functional groups for attachment via phosphoramidite chemistry.
- this type of reaction creating polymers of ETMs either as a portion of the backbone of the nucleic acid or as "side groups" of the nucleic acids, to allow amplification of the signals generated herein, can be done with virtually any ETM that can be functionalized to contain the correct chemical groups.
- nucleic acid analogs are made; that is, the invention provides nucleic acids having a backbone comprising at least one metallocene.
- a metallocene such as ferrocene (or other ETMs)
- the invention provides nucleic acids having a backbone comprising at least one metallocene.
- nucleic acids having metallocenes attached to the backbone i.e. via a ribose, a phosphate, etc. That is, two nucleic acids each made up of a traditional nucleic acid or analog (nucleic acids in this case including a single nucleoside), may be covalently attached to each other via a metallocene.
- a metallocene derivative or substituted metallocene is provided, wherein each of the two aromatic rings of the metallocene has a nucleic acid substitutent group.
- metallocene polymers that is, there are areas of metallocene polymers within the backbone.
- nucleic acid substitutent groups it is also desirable in some instances to add additional substituent groups to one or both of the aromatic rings of the metallocene (or ETM).
- ETM metallocene
- these nucleoside replacements are generally part of probe sequences to be hybridized with a substantially complementary nucleic acid, for example a target sequence or another probe sequence
- substitutent groups to the metallocene rings to facilitate hydrogen bonding to the base or bases on the opposite strand. These may be added to any position on the metallocene rings.
- Suitable substitutent groups include, but are not limited to, amide groups, amine groups, carboxylic acids, and alcohols, including substituted alcohols.
- these substitutent groups can be attached via linkers as well, although in general this is not preferred.
- substituent groups on an ETM may be added to alter the redox properties of the ETM.
- metallocenes such as ferrocene
- substituent groups on an ETM may be added to alter the redox properties of the ETM.
- substituent groups on the metallocene may allow two different ETMs to be distinguished.
- the intermediate components are also provided.
- the invention provides phosphoramidite metallocenes, as generally depicted in Structure 39:
- PG is a protecting group, generally suitable for use in nucleic acid synthesis, with DMT, MMT and TMT all being preferred.
- the aromatic rings can either be the rings of the metallocene, or aromatic rings of ligands for transition metal complexes or other organic ETMs.
- the aromatic rings may be the same or different, and may be substituted as discussed herein.
- Structure 40 depicts the ferrocene derivative:
- Structure 41 depicts the ferrocene peptide nucleic acid (PNA) monomer, that can be added to PNA synthesis as is known in the art:
- the PG protecting group is suitable for use in peptide nucleic acid synthesis, with MMT, boc and Fmoc being preferred.
- ETM or metallocene polymers which are added to the nucleic acids, rather than as backbone replacements, as is more fully described below.
- the ETMs are attached as polymers, for example as metallocene polymers, in a "branched" configuration similar to the "branched DNA” embodiments herein and as outlined in U.S. Patent No. 5,124,246, using modified functionalized nucleotides.
- the general idea is as follows. A modified phosphoramidite nucleotide is generated that can ultimately contain a free hydroxy group that can be used in the attachment of phosphoramidite ETMs such as metallocenes. This free hydroxy group could be on the base or the backbone, such as the ribose or the phosphate (although as will be appreciated by those in the art, nucleic acid analogs containing other structures can also be used).
- the modified nucleotide is incorporated into a nucleic acid, and any hydroxy protecting groups are removed, thus leaving the free hydroxyl.
- a phosphoramidite ETM such as a metallocene
- ETMs such as metallocene ETMs
- Additional phosphoramidite ETMs such as metallocenes can be added, to form "ETM polymers", including "metallocene polymers” as depicted herein, particularly for ferrocene.
- solubility of the polymers by adding a "capping" group to the terminal ETM in the polymer, for example a final phosphate group to the metallocene as is generally depicted in Figure 12.
- a "capping" group to the terminal ETM in the polymer, for example a final phosphate group to the metallocene as is generally depicted in Figure 12.
- Other suitable solubility enhancing "capping" groups will be appreciated by those in the art. It should be noted that these solubility enhancing groups can be added to the polymers in other places, including to the ligand rings, for example on the metallocenes as discussed herein
- the 2' position of a ribose of a phosphoramidite nucleotide is first functionalized to contain a protected hydroxy group, in this case via an oxo-linkage, although any number of linkers can be used, as is generally described herein for Z linkers.
- the protected modified nucleotide is then incorporated via standard phosphoramidite chemistry into a growing nucleic acid.
- the protecting group is removed, and the free hydroxy group is used, again using standard phosphoramidite chemistry to add a phosphoramidite metallocene such as ferrocene.
- a similar reaction is possible for nucleic acid analogs. For example, using peptide nucleic acids and the metallocene monomer shown in Structure 41 , peptide nucleic acid structures containing metallocene polymers could be generated.
- the present invention provides recruitment linkers of nucleic acids comprising "branches" of metallocene polymers as is generally depicted in Figures 12 and 13.
- Preferred embodiments also utilize metallocene polymers from one to about 50 metallocenes in length, with from about 5 to about 20 being preferred and from about 5 to about 10 being especially preferred.
- the recruitment linker is nucleic acid
- any combination of ETM attachments may be done.
- the recruitment linker is not nucleic acid, and instead may be any sort of linker or polymer.
- linker or polymer that can be modified to contain ETMs can be used.
- the polymers or linkers should be reasonably soluble and contain suitable functional groups for the addition of ETMs.
- a "recruitment polymer" comprises at least two or three subunits, which are covalently attached. At least some portion of the monomeric subunits contain functional groups for the covalent attachment of ETMs.
- coupling moieties are used to covalently link the subunits with the ETMs.
- Preferred functional groups for attachment are amino groups, carboxy groups, oxo groups and thiol groups, with amino groups being particularly preferred.
- a wide variety of recruitment polymers are possible.
- Suitable linkers include, but are not limited to, alkyl linkers (including heteroalkyl (including (poly)ethylene glycol-type structures), substituted alkyl, aryalkyl linkers, etc.
- the linkers will comprise one or more functional groups for the attachment of ETMs, which will be done as will be appreciated by those in the art, for example through the use homo-or hetero- bifunctional linkers as are well known (see 1994 Pierce Chemical Company catalog, technical section on cross-linkers, pages 155-200, incorporated herein by reference).
- Suitable recruitment polymers include, but are not limited to, functionalized styrenes, such as amino styrene, functionalized dextrans, and polyamino acids.
- Preferred polymers are polyamino acids (both poly-D-amino acids and poly-L-amino acids), such as polylysine, and polymers containing lysine and other amino acids being particularly preferred.
- Other suitable polyamino acids are polyglutamic acid, polyaspartic acid, co-polymers of lysine and glutamic or aspartic acid, co-polymers of lysine with alanine, tyrosine, phenylalanine, serine, tryptophan, and/or proline.
- the recruitment linker comprises a metallocene polymer, as is described above.
- the attachment of the recruitment linkers to the first portion of the label probe will depend on the composition of the recruitment linker, as will be appreciated by those in the art.
- the recruitment linker is nucleic acid, it is generally formed during the synthesis of the first portion of the label probe, with incorporation of nucleosides containing ETMs as required.
- the first portion of the label probe and the recruitment linker may be made separately, and then attached. For example, there may be an overlapping section of complementarity, forming a section of double stranded nucleic acid that can then be chemically crosslinked, for example by using psoralen as is known in the art.
- attachment of the linker/polymer of the recruitment linker will be done generally using standard chemical techniques, such as will be appreciated by those in the art.
- attachment can be similar to the attachment of insulators to nucleic acids.
- recruitment linkers that are mixtures of nucleic acids and non-nucleic acids, either in a linear form (e.g. nucleic acid segments linked together with alkyl linkers) or in branched forms (nucleic acids with alkyl "branches" that may contain ETMs and may be additionally branched).
- the target sequence itself that carries the ETMs, rather than the recruitment linker of a label probe.
- PCR polymerase chain reaction
- preferred attachments in this embodiment are to the base or ribose of the nucleotide.
- PCR amplification of a target sequence will result in target sequences comprising ETMs, generally randomly incorporated into the sequence.
- the system of the invention can then be configured to allow detection using these ETMs, as is generally depicted in Figures 16A, 16B and 16D of U.S.S.N. 60/190,259.
- compositions utilizing electrodes comprising monolayers of conductive oligomers and capture probes, and target sequences that comprise a first portion that is capable of hybridizing to a component of an assay complex, and a second portion that does not hybridize to a component of an assay complex and comprises at least one covalently attached electron transfer moiety.
- methods utilizing these compositions are also provided.
- ETMs connected to probe sequences, i.e. sequences designed to hybridize to complementary sequences.
- ETMs may be added to non-recruitment linkers as well.
- ETMs may be added to sections of label probes that do hybridize to components of the assay complex, for example the first portion, or to the target sequence as outlined above.
- These ETMs may be used for electron transfer detection in some embodiments, or they may not, depending on the location and system.
- the target sequence containing randomly incorporated ETMs is hybridized directly to the capture probe, as is depicted in Figure 16Aof U.S.S.N.
- ETMs there may be ETMs in the portion hybridizing to the capture probe. If the capture probe is attached to the electrode using a conductive oligomer, these ETMs can be used to detect electron transfer as has been previously described. Alternatively, these ETMs may not be specifically detected.
- the recruitment linker when the recruitment linker is nucleic acid, it may be desirable in some instances to have some or all of the recruitment linker be double stranded.
- the first recruitment linker comprises the covalently attached ETMs.
- the second recruitment linker contains the ETMs, and the first recruitment linker does not, and the ETMs are recruited to the surface by hybridization of the second recruitment linker to the first.
- both the first and second recruitment linkers comprise ETMs.
- nucleic acids comprising a large number of ETMs may not hybridize as well, i.e. the T m may be decreased, depending on the site of attachment and the characteristics of the ETM.
- the T m may be decreased, depending on the site of attachment and the characteristics of the ETM.
- the ETMs when multiple ETMs are used on hybridizing strands, generally there are less than about 5, with less than about 3 being preferred, or alternatively the ETMs should be spaced sufficiently far apart that the intervening nucleotides can sufficiently hybridize to allow good kinetics.
- non-covalently attached ETMs may be used.
- the ETM is a hybridization indicator.
- Hybridization indicators serve as ETMs that will preferentially associate with double stranded nucleic acid, usually reversibly, similar to the method of Millan et al., Anal. Chem. 65:2317-2323 (1993); Millan et al., Anal. Chem. 662943-2948 (1994), both of which are hereby expressly incorporated by reference.
- increases in the local concentration of ETMs, due to the association of the ETM hybridization indicator with double stranded nucleic acid at the surface can be monitored using the monolayers comprising the conductive oligomers.
- Hybridization indicators include intercalators and minor and/or major groove binding moieties.
- intercalators may be used; since intercalation generally only occurs in the presence of double stranded nucleic acid, only in the presence of double stranded nucleic acid will the ETMs concentrate. Intercalating transition metal complex ETMs are known in the art. Similarly, major or minor groove binding moieties, such as methylene blue, may also be used in this embodiment.
- the systems of the invention may utilize non-covalently attached ETMs, as is generally described in Napier et al., Bioconj. Chem. 8:906 (1997), hereby expressly incorporated by reference.
- ETMs changes in the redox state of certain molecules as a result of the presence of DNA (i.e. guanine oxidation by ruthenium complexes) can be detected using SAMs comprising conductive oligomers.
- the present invention provides electrodes comprising monolayers comprising conductive oligomers, generally including capture probes, and either target sequences or label probes comprising recruitment linkers containing ETMs.
- Probes of the present invention are designed to be complementary to a target sequence (either the target sequence of the sample or to other probe sequences, as is described below), such that hybridization of the target sequence and the probes of the present invention occurs.
- this complementarity need not be perfect; there may be any number of base pair mismatches which will interfere with hybridization between the target sequence and the single stranded nucleic acids of the present invention.
- the sequence is not a complementary target sequence.
- substantially complementary herein is meant that the probes are sufficiently complementary to the target sequences to hybridize under normal reaction conditions.
- the nucleic acid compositions of the invention are useful as oligonucleotide probes.
- the length of the probe will vary with the length of the target sequence and the hybridization and wash conditions.
- oligonucleotide probes range from about 8 to about 50 nucleotides, with from about 10 to about 30 being preferred and from about 12 to about 25 being especially preferred. In some cases, very long probes may be used, e.g. 50 to 200-300 nucleotides in length.
- nucleosides may be replaced with nucleic acids.
- hybridization conditions may be used in the present invention, including high, moderate and low stringency conditions; see for example Maniatis et al., Molecular Cloning: A Laboratory Manual, 2d Edition, 1989, and Short Protocols in Molecular Biology, ed. Ausubel, et al, hereby incorporated by referenece.
- the hybridization conditions may also vary when a non-ionic backbone, e.g. PNA is used, as is known in the art.
- cross-linking agents may be added after target binding to cross-link, i.e. covalently attach, the two strands of the hybridization complex.
- the systems of the invention may take on a large number of different configurations, as is generally depicted in the Figures of U.S.S.N. 09/626,096 (the Figures in the next paragraphs refer to the figures of U.S.S.N. 09/626,096).
- systems in which the target sequence itself is labeled with ETMs see Figures 16A, 16B and 16D
- systems in which label probes directly hybridize to the target sequences see Figures 16C and 16H
- systems in which label probes are indirectly hybridized to the target sequences for example through the use of amplifier probes (see Figures 16E, 16F and 16G).
- the invention provides assay complexes that minimally comprise a target analyte and a capture binding ligand.
- assay complex herein is meant the collection of hybridization complexes comprising nucleic acids, including probes and targets, that contains at least one label (preferably an ETM in the electronic methods of the present invention) and thus allows detection.
- the composition of the assay complex depends on the use of the different probe components outlined herein.
- the assay complexes may also include label probes, capture extender probes, label extender probes, and amplifier probes, as outlined herein and in U.S.S.N. 09/626,096, depending on the configuration used. ⁇
- the assays are generally run under stringency conditions which allow formation of the label probe hybridization complex only in the presence of target.
- Stringency can be controlled by altering a step parameter that is a thermodynamic variable, including, but not limited to, temperature, formamide concentration, salt concentration, chaotropic salt concentration pH, organic solvent concentration, etc.
- reaction may be accomplished in a variety of ways, as will be appreciated by those in the art. Components of the reaction may be added simultaneously, or sequentially, in any order, with preferred embodiments outlined below.
- the reaction may include a variety of other reagents. These include reagents like salts, buffers, neutral proteins (e.g. albumin), detergents, etc which may be used to facilitate optimal hybridization and detection, and/or reduce non-specific or background interactions. Also reagents that otherwise improve the efficiency of the assay, such as protease inhibitors, nuclease inhibitors, anti-microbial agents, etc., may be used, depending on the sample preparation methods and purity of the target.
- the present invention provides biochips, with covalently attached capture binding ligands (e.g. capture probes).
- the biochips are incorporated into the cartridges of the invention and then fitted into the stations of the multiplexing devices of the invention for running assays.
- the biochips are attached to the rest of the cartridge in a wide variety of ways.
- the biochip is made directly on a portion of the cartridge and is thus incorporated into the system.
- attachment mechanisms that can be used, depending on the composition and configuration of the two substrates.
- the biochip when the biochip is formulated on printed circuit board material, there can be "pins" or “rods” that are inserted into holes, with subsequent fusion (for example, using solvents or heat). Similarly, surface-to-surface heat or solvent fusion may be done.
- adhesives can be used to glue the two together. Similarly, these techniques can be used with additional sealing components such as gaskets.
- the biochip may "snap" into the cartridge, using components such as molded plastic snapping devices.
- the present invention further provides for holders for the cartridges for loading with samples, prior to loading the cartridges into the stations of the device.
- the holders may be configured in a wide variety of ways, depending on the configuration of the cartridges and caps, if present. For example, holders that align cartridges such that standard reagent handling tools can be used are preferred. As shown in the Figures, holders that allow the use of mullfichannel pipettemen or robotic systems based on 96 well formats are preferred.
- the holders may also include the caps, positioned for easy use, or reagents and/or buffer components. In general, the holders are fabricated out of materials resistant to the chemicals and reagents used in the assays.
- the cartridges of the invention are designed to be inserted into stations in a multiplexing device.
- the devices of the invention can take on a wide variety of conformations, depending on the desired components, the end use, the ultimate desired size of the instrument, etc.
- Each multiplexing device has a number of different stations into which the cartridges are inserted.
- the cartridge/station pair can be configured in a variety of ways to include the use of "snap-in" locks, asymmetry such that the cartridge only fits into the device in a particular orientation, different size stations for different size cartridges (for example, some rare amount of tests may require special handling and the machines may be designed with special stations for these tests).
- This embodiment may also utilize electronic sensors that detect the presence or absence of a cartridge, or whether the cartridge is correctly positioned.
- the number of stations per device will vary with the desired use. Preferred embodiments utilize at least two or three stations, with at least 5 - 100 being preferred, and from about 25-50 being particularly preferred, with 48 being especially preferred.
- the devices are laid out as a matrix, with columns and rows of stations.
- each station can have a number of different functional components, including, but not limited to, interconnects to electronic components, thermocontrollers, signaling systems, sensors for leak detection, alphanumeric displays, and detectors.
- the stations comprise matching interconnects for the biochip, to allow electronic communication between the chip and the device.
- each station comprises an individual thermal controller.
- "Thermal controller” or “thermocontroller” in this context includes elements that can both heat and cool the cartridges and thus the samples in the cartridges as well. In general, given the size and function of the systems, it is desirable to utilize small, fast thermocontrollers. There are a wide variety of known suitable thermocontrollers, including Peltier systems.
- thermocontroller should be able to heat/cool samples ranging from 0 to about 100°C and at a rate ranging from 0.01°C/sec to 10°C/sec.
- thermocontroller can be used after an assay to destroy the biological material in the cartridge. That is, it is frequently desirable to minimize the exposure of health care workers and lab workers to potentially dangerous samples, and to facilitate the disposal of these materials.
- the thermocontroller can be used to heat the spent sample at extreme temperatures for some period of time in order to kill or destroy the sample. In addition, heating in conjunction with the addition of other generally harsh reagents (strong acid, strong base, etc.) can also be used.
- an RF antennae is used to generate plasma that is pumped into the chamber after fluid evacuation to destroy all biological material.
- each station comprising an individual thermal controller
- sets (for example, rows or columns) of the stations share a thermal controller.
- the multiplexing device comprises a single thermal controller.
- the devices of the invention include a "Stat Slot", where a cartridge can be put in and read right away at one station, rather than run as a sequence.
- the temperature at this station may be preset.
- the stations of the device include signaling systems.
- a system of lights, particularly colored lights, at each station can be used to indicate the status of the cartridge or the assay: cartridge present or absent, assay in progress, error, assay completed, etc.
- the configuration of the lights may be the code (particularly for color blind people); two lights for cartridge in, flashing lights for assay finished, etc.
- these signaling systems may be at each station or at sets of stations.
- the devices of the invention include an alphanumeric display to allow the display of data or other information.
- this display may be used in conjunction with a barcode reader, described below, to show the operator which cartridge was inserted (e.g. the HIV panel, the HCV panel, the infectious disease panel, the breast cancer SNP panel, etc.), or other data about the cartridge (lot or batch number, etc.).
- the display can be used to give the operator the test results, etc.
- a display can be at each station, or there may be displays for sets of stations or for the whole device.
- each station of the device may be configured to allow electrophoresis or dielectrophoresis on the biochip. That is, as is generally described in W099/67425 and U.S.S.N. 09/171,981, hereby incorporated by reference, there may be additional electrodes or electronic components to allow the concentration and/or movement of analytes to the surface of the array. Similarly, as is described in W099/67425 and U.S.S.N. 09/171,981, the electrophoresis or dielectrophoresis electrodes may be contained on the biochip.
- the device (or alternatively, each station) comprises a barcode reader to read a corresponding barcode on the cartridge.
- barcodes may be used for a wide variety of purposes, including, but not limited to, identifying the sample (e.g. patient number or code), the test being done, the batch number of the chip, calibration information, assay protocols including cycle time, signal processing requirements, etc.
- the barcode can be used to control the instrument.
- instrument control may be through the use of a keyboard, a mouse or a barcode reader.
- barcodes on the cartridges to indicate the identity of the chip, but also on a card to scan for starting the assay, stopping the assay, downloading the data, etc.
- the card of barcode commands are found in a drawer or storage compartment of the device, outlined herein.
- each station comprises a memory chip reader.
- each cartridge comprises a memory chip, that can have sample information (e.g. patient number or code), the test being done, the batch number of the chip, calibration information, assay protocols, etc.), or what the user interface looks like (for example, not a number but "HIV positive”), etc.
- each station comprises a memory chip writer to add information to the cartridge, such as what test was done, the date, the results, etc.
- each station has encryption components in conjunction with the cartridge, to encrypt patient information.
- the devices of the invention will not allow the operator to know the results of the test. Rather, the output will be a confirmation that the test was performed correctly and a viable answer received, but will say nothing about the actual test being done or the results.
- the test results themselves, in addition to the patient information, can be encrypted and sent to a remote location as outlined below for processing, decryption or storage.
- the device may include drawers or storage compartments to allow the storage of reagents, cartridges, caps, holders, pipettemen, etc.
- the device comprises a reader at each station.
- the device comprises a single reader that is moved, either by moving the reader or by moving the stations to a single reader within the device.
- the devices of the invention comprise liquid handling components, including components for loading and unloading fluids at each station or sets of stations.
- the liquid handling systems can include robotic systems comprising any number of components.
- any or all of the steps outlined herein may be automated; thus, for example, the systems may be completely or partially automated.
- components which can be used, including, but not limited to, one or more robotic arms; plate handlers for the positioning of microplates; holders with cartridges and/or caps; automated lid or cap handlers to remove and replace lids for wells on non-cross contamination plates; tip assemblies for sample distribution with disposable tips; washable tip assemblies for sample distribution; 96 well loading blocks; cooled reagent racks; microtitler plate pipette positions (optionally cooled); stacking towers for plates and tips; and computer systems.
- Fully robotic or microfluidic systems include automated liquid-, particle-, cell- and organism-handling including high throughput pipetting to perform all steps of screening applications.
- This includes liquid, particle, cell, and organism manipulations such as aspiration, dispensing, mixing, diluting, washing, accurate volumetric transfers; retrieving, and discarding of pipet tips; and repetitive pipetting of identical volumes for multiple deliveries from a single sample aspiration.
- These manipulations are cross-contamination-free liquid, particle, cell, and organism transfers.
- This instrument performs automated replication of microplate samples to filters, membranes, and/or daughter plates, high- density transfers, full-plate serial dilutions, and high capacity operation.
- chemically derivatized particles, plates, cartridges, tubes, magnetic particles, or other solid phase matrix with specificity to the assay components are used.
- the binding surfaces of microplates, tubes or any solid phase matrices include non-polar surfaces, highly polar surfaces, modified dextran coating to promote covalent binding, antibody coating, affinity media to bind fusion proteins or peptides, surface-fixed proteins such as recombinant protein A or G, nucleotide resins or coatings, and other affinity matrix are useful in this invention.
- platforms for multi-well plates, multi-tubes, holders, cartridges, minitubes, deep-well plates, microfuge tubes, cryovials, square well plates, filters, chips, optic fibers, beads, and other solid-phase matrices or platform with various volumes are accommodated on an upgradable modular platform for additional capacity.
- This modular platform includes a variable speed orbital shaker, and multi-position work decks for source samples, sample and reagent dilution, assay plates, sample and reagent reservoirs, pipette tips, and an active wash station.
- thermocycler and thermoregulating systems are used for stabilizing the temperature of heat exchangers such as controlled blocks or platforms to provide accurate temperature control of incubating samples from 0°C to 100°C; this is in addition to or in place of the station thermocontrollers.
- interchangeable pipet heads with single or multiple magnetic probes, affinity probes, or pipetters robotically manipulate the liquid, particles, cells, and organisms.
- Multi-well or multi-tube magnetic separators or platforms manipulate liquid, particles, cells, and organisms in single or multiple sample formats.
- the instrumentation will include a detector, which can be a wide variety of different detectors, depending on the labels and assay.
- useful detectors include a microscope(s) with multiple channels of fluorescence; plate readers to provide fluorescent, ultraviolet and visible spectrophotometric detection with single and dual wavelength endpoint and kinetics capability, fluroescence resonance energy transfer (FRET), luminescence, quenching, two-photon excitation, and intensity redistribution; CCD cameras to capture and transform data and images into quantifiable formats; and a computer workstation.
- the living cells may be grown under controlled growth conditions, with controls for temperature, humidity, and gas for time series of the live cell assays. Automated transformation of cells and automated colony pickers may facilitate rapid screening of desired cells.
- Flow cytometry or capillary electrophoresis formats can be used for individual capture of magnetic and other beads, particles, cells, and organisms.
- the flexible hardware and software allow instrument adaptability for multiple applications.
- the software program modules allow creation, modification, and running of methods.
- the system diagnostic modules allow instrument alignment, correct connections, and motor operations.
- the customized tools, labware, and liquid, particle, cell and organism transfer patterns allow different applications to be performed.
- the database allows method and parameter storage. Robotic and computer interfaces allow communication between instruments.
- the robotic apparatus includes a central processing unit which communicates with a memory and a set of input/output devices (e.g., keyboard, mouse, monitor, printer, etc.) through a bus. Again, as outlined below, this may be in addition to or in place of the CPU for the multiplexing devices of the invention.
- a central processing unit which communicates with a memory and a set of input/output devices (e.g., keyboard, mouse, monitor, printer, etc.) through a bus.
- input/output devices e.g., keyboard, mouse, monitor, printer, etc.
- this may be in addition to or in place of the CPU for the multiplexing devices of the invention.
- the general interaction between a central processing unit, a memory, input/output devices, and a bus is known in the art. Thus, a variety of different procedures, depending on the experiments to be run, are stored in the CPU memory.
- robotic fluid handling systems can utilize any number of different reagents, including buffers, reagents, samples, washes, assay components such as label probes, etc.
- the devices of the invention include sensors for leak detection. These are generally of two types; either electronic measurements of resistance or the spiking of the assay with optical or detectable tags. This may be particularly important in some embodiments where biohazardous materials or caustic chemicals are being tested.
- the devices of the invention comprise a device board that can be used to do a variety of analyses, including signal processing, digital lock-in, comprising logic circuits, etc., as outlined herein.
- the devices of the invention comprise a device board that can be used to do a variety of analyses, including signal processing, digital lock-in, comprising logic circuits, etc., as outlined herein.
- the systems of the invention comprise a processor or central processing unit (CPU) with an associated memory.
- the associated memory can be memory on-board the processor and optional memory coupled to the processor via an external memory bus.
- This processor (CPU) can be physically contained within the apparatus itself, can be connected to the apparatus via a cable, or can be connected using wireless technology. There can be one or more per device or one can be shared among devices.
- the systems of the invention provide a motherboard on which are mounted the CPU and associated memory.
- the motherboard may desirably provide connectors for mechanically and electrically connecting with one or a plurality of edge connector mountable printed circuit cards having the signal processing circuits formed thereon.
- the edge connectors provide signal and power connections with the motherboard.
- the CPU and memory in conjunction with an operating system, support the menu or command driven operation and analysis described elsewhere herein.
- Software and/or firmware executing in the processor and/or within the signal processing printed circuit card components are used to control the operation of the apparatus, devices, and system.
- each signal processing printed circuit card may be connected to the personal computer by a separate communication channel or link (such as for example, by one or more serial, parallel, SCSI, Fire-wire, blue-tooth, or other wired or wireless communication channel or link), or multiple signal processing printed circuit cards may be multiplexed to share a smaller number of communication channels or links.
- the multiple signal processing printed circuit cards will interconnect via a communication bus, such as may be provided by a motherboard or other interconnect structure.
- Each signal processing board may have a unique address (locally or globally unique) such that communications directed between signal processing cards or between a signal processing printed circuit card to the processor may be identified with the signal processing card and interpreted and/or routed accordingly.
- the PC contains an application program that controls the instrument and collects data from the instrument.
- an apparatus having six sensor slots on each of eight separate printed circuit based signal processing cards is coupled with a personal computer via at least one serial interface, such as an RS-232 or RS-485 serial link.
- a serial interface such as an RS-232 or RS-485 serial link.
- a plurality of such serial ports on each of the personal computer and apparatus are provided to increase bandwidth.
- three serial input/output interfaces are provided.
- a processor or CPU with associated memory may be provided directly one each signal processing printed board.
- the devices of the invention include a localization device, such as a Global Positioning System (GPS) as are known in the art. This may find particular use in agriculture and biowarfare uses, as well as remote diagnosis of problems.
- GPS Global Positioning System
- the devices of the invention include components for the communication of data, assay results, patient information, etc. to an off-device location.
- one or more modems including both telephone and cable modems
- internet cards including both telephone and cable modems
- infrared ports may be included in the devices to allow the transmission of data and other relevant information (barcode information, assay conditions and protocols, operator identification, time stamps, etc.) to a remote location such as a general information repository, hospitals, doctor's offices, epidemiology centers, pharmacies, government centers, insurance providers, etc.
- the devices of the invention include components for wireless communication systems, to allow this transmission of data in the absence of physical electronic or communications connections.
- wireless receivers can be included.
- the present invention provides methods and compositions for the multiplex analysis of samples and target analytes.
- Samples either raw samples or treated samples (e.g. amplified, purified, etc.)
- optional caps are put on, and the cartridges loaded into a station of the device. Additional reagents are added as necessary, and assay complexes formed.
- detection proceeds with electronic initiation. Without being limited by the mechanism or theory, detection is based on the transfer of electrons from the ETM to the electrode.
- Detection of electron transfer i.e. the presence of the ETMs, is generally initiated electronically, with voltage being preferred.
- a potential is applied to the assay complex. Precise control and variations in the applied potential can be via a potentiostat and either a three electrode system (one reference, one sample (or working) and one counter electrode) or a two electrode system (one sample and one counter electrode). This allows matching of applied potential to peak potential of the system which depends in part on the choice of ETMs and in part on the other system components, the composition and integrity of the monolayer, and what type of reference electrode is used. As described herein, ferrocene is a preferred ETM.
- co-reductants or co-oxidants are used as is generally described in WO00/16089, hereby expressly incorporated by reference.
- the presence of the ETMs at the surface of the monolayer can be detected in a variety of ways.
- a variety of detection methods may be used, including, but not limited to, optical detection (as a result of ' spectral changes upon changes in redox states), which includes fluorescence, phosphorescence, luminiscence, chemiluminescence, electrochemiluminescence, and refractive index; and electronic detection, including, but not limited to, amperommetry, voltammetry, capacitance and impedence.
- optical detection as a result of ' spectral changes upon changes in redox states
- electronic detection including, but not limited to, amperommetry, voltammetry, capacitance and impedence.
- These methods include time or frequency dependent methods based on AC or DC currents, pulsed methods, lock-in techniques, filtering (high pass, low pass, band pass), and time-resolved techniques including time-resolved fluoroscence.
- the efficient transfer of electrons from the ETM to the electrode results in stereotyped changes in the redox state of the ETM.
- ETMs including the complexes of ruthenium containing bipyridine, pyridine and imidazole rings
- these changes in redox state are associated with changes in spectral properties.
- Significant differences in absorbance are observed between reduced and oxidized states for these molecules. See for example Fabbrizzi et al., Chem. Soc. Rev. 1995 pp197-202). These differences can be monitored using a spectrophotometer or simple photomultiplier tube device.
- possible electron donors and acceptors include all the derivatives listed above for photoactivation or initiation.
- Preferred electron donors and acceptors have characteristically large spectral changes upon oxidation and reduction resulting in highly sensitive monitoring of electron transfer.
- Such examples include Ru(NH 3 ) 4 py and Ru(bpy) 2 im as preferred examples. It should be understood that only the donor or acceptor that is being monitored by absorbance need have ideal spectral characteristics.
- the electron transfer is detected fluorometrically.
- Numerous transition metal complexes, including those of ruthenium, have distinct fluorescence properties. Therefore, the change in redox state of the electron donors and electron acceptors attached to the nucleic acid can be monitored very sensitively using fluorescence, for example with Ru(4J-biphenyl 2 -phenanthroline) 3 2+ . The production of this compound can be easily measured using standard fluorescence assay techniques.
- laser induced fluorescence can be recorded in a standard single cell fluorimeter, a flow through "on-line” fluorimeter (such as those attached to a chromatography system) or a multi-sample “plate-reader” similar to those marketed for 96-well immuno assays.
- fluorescence can be measured using fiber optic sensors with nucleic acid probes in solution or attached to the fiber optic. Fluorescence is monitored using a photomultiplier tube or other light detection instrument attached to the fiber optic. The advantage of this system is the extremely small volumes of sample that can be assayed.
- scanning fluorescence detectors such as the Fluorimager sold by Molecular Dynamics are ideally suited to monitoring the fluorescence of modified nucleic acid molecules arrayed on solid surfaces.
- the advantage of this system is the large number of electron transfer probes that can be scanned at once using chips covered with thousands of distinct nucleic acid probes.
- transition metal complexes display fluorescence with large Stokes shifts. Suitable examples include bis- and trisphenanthroline complexes and bis- and trisbipyridyl complexes of transition metals such as ruthenium (see Juris, A., Balzani, V., et. al. Coord. Chem. Rev., V. 84, p. 85-277, 1988). Preferred examples display efficient fluorescence (reasonably high quantum yields) as well as low reorganization energies.
- electrochemiluminescence is used as the basis of the electron transfer detection.
- ETMs such as Ru 2+ (bpy) 3
- direct luminescence accompanies excited state decay. Changes in this property are associated with nucleic acid hybridization and can be monitored with a simple photomultiplier tube arrangement (see Blackburn, G. F. Clin. Chem. 37: 1534-1539 (1991); and Juris et al., supra.
- electronic detection is used, including amperommetry, voltammetry, capacitance, and impedence.
- Suitable techniques include, but are not limited to, electrogravimetry; coulometry (including controlled potential coulometry and constant current coulometry); voltammetry (cyclic voltammetry, pulse voltammetry (normal pulse voltammetry, square wave voltammetry, differential pulse voltammetry, Osteryoung square wave voltammetry, and coulostatic pulse techniques); stripping analysis (aniodic stripping analysis, cathiodic stripping analysis, square wave stripping voltammetry); conductance measurements (electrolytic conductance, direct analysis); time- dependent electrochemical analyses (chronoamperometry, chronopotentiometry, cyclic chronopotentiometry and amperometry, AC polography, chronogalvametry, and chronocoulometry); AC impedance measurement; capacitance measurement; AC voltammetry; and photoelectrochemistry.
- monitoring electron transfer is via amperometric detection.
- This method of detection involves applying a potential (as compared to a separate reference electrode) between the nucleic acid-conjugated electrode and a reference (counter) electrode in the sample containing target genes of interest. Electron transfer of differing efficiencies is induced in samples in the presence or absence of target nucleic acid; that is, the presence or absence of the target nucleic acid, and thus the label probe, can result in different currents.
- the device for measuring electron transfer amperometrically involves sensitive current detection and includes a means of controlling the voltage potential, usually a potentiostat. This voltage is optimized with reference to the potential of the electron donating complex on the label probe.
- Possible electron donating complexes include those previously mentioned with complexes of iron, osmium, platinum, cobalt, rhenium and ruthenium being preferred and complexes of iron being most preferred.
- potentiometric (or voltammetric) measurements involve non-faradaic (no net current flow) processes and are utilized traditionally in pH and other ion detectors. Similar sensors are used to monitor electron transfer between the ETM and the electrode.
- other properties of insulators and of conductors such as resistance conductivity, impedance and capicitance could be used to monitor electron transfer between ETM and the electrode.
- any system that generates a current such as electron transfer
- also generates a small magnetic field which may be monitored in some embodiments.
- one benefit of the fast rates of electron transfer observed in the compositions of the invention is that time resolution can greatly enhance the signal-to-noise results of monitors based on absorbance, fluorescence and electronic current.
- the fast rates of electron transfer of the present invention result both in high signals and stereotyped delays between electron transfer initiation and completion. By amplifying signals of particular delays, such as through the use of pulsed initiation of electron transfer and "lock-in" amplifiers of detection, and Fourier transforms.
- electron transfer is initiated using alternating current (AC) methods.
- AC alternating current
- ETMs bound to an electrode, generally respond similarly to an AC voltage across a circuit containing resistors and capacitors.
- techniques that can be used to increase the signal, decrease the noise, or make the signal more obvious or detectable in a background of noise. That is, any technique that can serve to better identify a signal in the background noise may find use in the present invention. These techniques are generally classified in three ways: (1) variations in the type or methods of applying the initiation signals (i.e. varying the "input" to maximize or identify the sample signal); (2) data processing, i.e.
- suitable "input" AC methods include, but are not limited to, using multiple frequencies; increasing the AC amplitude; the use of square wave ACV; the use of special or complicated waveforms; etc.
- suitable "output" AC techniques include, but are not limited to, monitoring higher harmonic frequencies; phase analysis or filters; background subtration techniques (including but not limited to impedance analysis and the use of signal recognition or peak recognition techniques); digital filtering techniques; bandwidth narrowing techniques (including lock-in detection schemes particularly digital lock in); Fast Fourier Transform (FFT) methods; correlation and/or convolution techniques; signal averaging; spectral analysis; etc.
- FFT Fast Fourier Transform
- varying components of the assay can be done to result in the sample signal and the noise signal being altered in a non-parallel fashion; that is, the two signals respond non-linearly with respect to each other.
- non-specifically bound label probes/ETMs show differences in impedance (e.g. higher impedances) than when the label probes containing the ETMs are specifically bound in the correct orientation.
- the non-specifically bound material is washed away, resulting in an effective impedance of infinity.
- frequency response when using AC initiation and detection methods, the frequency response of the system changes as a result of the presence of the ETM.
- frequency response herein is meant a modification of signals as a result of electron transfer between the electrode and the ETM. This modification is different depending on signal frequency.
- a frequency response includes AC currents at one or more frequencies, phase shifts, DC offset voltages, faradaic impedance, etc.
- the first input electrical signal is then applied to the system, preferably via at least the sample electrode (containing the complexes of the invention) and the counter electrode, to initiate electron transfer between the electrode and the ETM.
- the first input signal comprises at least an AC component.
- the AC component may be of variable amplitude and frequency. Generally, for use in the present methods, the AC amplitude ranges from about 1 mV to about 1.1 V, with from about 10 mV to about 800 mV being preferred, and from about 10 mV to about 500 mV being especially preferred.
- the AC frequency ranges from about 0.01 Hz to about 100 MHz, with from about 10 Hz to about 10 MHz being preferred, and from about 100 Hz to about 20 MHz being especially preferred.
- the first input signal comprises a DC component and an AC component. That is, a DC offset voltage between the working and counter electrodes is swept through the electrochemical potential of the ETM (for example, when ferrocene is used, the sweep is generally from 0 to 500 mV) (or alternatively, the working electrode is grounded and the counter electrode is swept from 0 to -500 mV).
- the sweep is used to identify the DC voltage at which the maximum response of the system is seen. This is generally at or about the electrochemical potential of the ETM. Once this voltage is determined, either a sweep or one or more uniform DC offset voltages may be used.
- DC offset voltages of from about -1 V to about +1.1 V are preferred, with from about -500 mV to about +800 mV being especially preferred, and from about -300 mV to about 500 mV being particularly preferred. In a preferred embodiment, the DC offset voltage is not zero.
- an AC signal component of variable amplitude and frequency is applied. If the ETM is present, and can respond to the AC perturbation, an AC current will be produced due to electron transfer between the electrode and the ETM.
- the devices of the invention preferably provide voltage sources capable of delivering both AC and DC currents.
- a single input signal may be applied to differentiate between the presence and absence of the ETM (i.e. the presence of the target sequence) nucleic acid.
- a plurality of input signals are applied. As outlined herein, this may take a variety of forms, including using multiple frequencies, multiple DC offset voltages, or multiple AC amplitudes, or combinations of any or all of these.
- DC offset voltages are used, although as outlined above, DC voltage sweeps are preferred. This may be done at a single frequency, or at two or more frequencies.
- the AC frequency is varied.
- different molecules respond in different ways.
- increasing the frequency generally increases the output current.
- higher frequencies result in a loss or decrease of output signal.
- the frequency will be greater than the rate of electron transfer between the ETM and the electrode, and then the output signal will also drop.
- multiple frequencies with a small AC voltage is applied and the fundamental of each is evaluated.
- a preferred embodiment utilizes several frequencies with a large AC voltage, and the harmonics of each are evaluated.
- preferred embodiments utilize several frequencies with a large AC voltage where the effect of the different frequencies on the system can result in an output that is different from the sum of the outputs at individual frequencies.
- detection utilizes a single measurement of output signal at a single frequency. That is, the frequency response of the system in the absence of target sequence, and thus the absence of label probe containing ETMs, can be previously determined to be very low at a particular high frequency. Using this information, any response at a particular frequency, will show the presence of the assay complex. That is, any response at a particular frequency is characteristic of the assay complex. Thus, it may only be necessary to use a single input frequency, and any changes in frequency response is an indication that the ETM is present, and thus that the target sequence is present.
- the input signals and data processing steps are done to increase the non- linearity of the system. That is, for example, the ferrocene response reacts non-linearly, producing a harmonic response in the signal above that in the background; this harmonic signal from AC voltammetry is most likely the result of a harmonic distortion due to the nonlinear response of the electrochemical cell; see Yap, J. of Electroanalytical Chem. 454:33 (1998); hereby incorporated by reference. Thus, any techniques that increase this non-linearity are desirable. In a preferred embodiment, techniques are used to increase the higher harmonic signals; thus, frequency and phase-sensitive lock-in detection is performed at both the fundamental frequency of the applied waveform and also at multiples of the fundamental frequency (i.e.
- the higher harmonics or just one. Since the background capacitance responds relatively linearly to AC signals (a sine wave input AC voltage results in a relatively nondistorted sine wave output), very little upper harmonic current is produced in the background. This gives a dramatic increase in the signal to noise ratio. Thus, detection at the higher harmonic frequencies, particularly the third, fourth and fifth harmonics (although the harmonics from second to tenth or greater can also be used) is shown to result in dramatic suppression of the background currents associated with non-Faradaic processes (like double layer charging) that can overwhelm the signal from the target molecules. In this way, tthe evaluation of the system at higher harmonic frequencies and phases can lead to signficant improvements in the detection limits and clarity of signal. However, in some embodiments, the analysis of higher harmonics is not desired.
- one method of increasing the non-linear harmonic response is to increase or vary the amplitude of the AC perturbation, although this may also be used in monitoring the fundamental frequency as well.
- increasing the amplitude increases the driving force nonlinearly.
- the same system gives an improved response (i.e. higher output signals) at any single frequency through the use of higher overpotentials at that frequency.
- the amplitude may be increased at high frequencies to increase the rate of electron transfer through the system, resulting in greater sensitivity, ln addition, this may be used, for example, to induce responses in slower systems such as those that do not possess optimal spacing configurations.
- measurements of the system are taken at at least two separate amplitudes or overpotentials, with measurements at a plurality of amplitudes being preferred.
- changes in response as a result of changes in amplitude may form the basis of identification, calibration and quantification of the system.
- one or more AC frequencies can be used as well.
- harmonic square wave AC voltage is used; see Baranski et al., J. Electroanal. Chem. 373:157 (1994), incorporated herein by reference, although in some embodiments this is not preferred.
- square waves are easier to create digitally and the pulse shape of the square wave can allow for better discrimination against charging capacitance.
- sinusoidal harmonic AC voltammetry harmonic signals provide better signal to background since faradaic response can be more nonlinear than charging capacitance.
- SW harmonic AC voltage The key difference between the two techniques is the frequency spectrum of the AC waveform.
- a singular frequency sinusoidal waveform contains just the fundamental frequency whereas a singular square wave contains the fundamental frequency as well as all odd harmonics.
- the technique looks at the even harmonics where the ratio of faradaic current to capacitance current is enhanced. All the odd harmonics have single AC voltage peaks while all the even harmonics have double AC voltage peaks. This is opposite to the case of sinusoidal harmonic AC voltage of a system that has a non-reversible redox couple.
- multiple frequency AC voltage is used.
- the idea is to create a waveform consisting of multiple frequencies with the same amplitude or different amplitudes to excite an electrochemical cell in an AC voltage fashion.
- the method benefits from fast Fourier transform or joint time-frequency transform to analyze the cell response.
- a JTFT spectrogram of a multiple frequencies AC voltage provides information on the driven (or fundamental) frequencies as well as their harmonic components.
- a fast Fourier transform is done, as is generally outlined in the examples.
- Fourier transform analysis is a preferred method for improving signal to noise and isolating desired signals when sinusoidal electrochemistry is done.
- Typical AC techniques rely on measurements of the primary frequency only.
- sinusoidal voltammetry (and other inputs) observation at higher harmonics allows discrimination of signals primarily based on kinetics. For example, both fast and slow redox events would give similar peaks (provided the AC frequency was not too high) at the primary frequency. However, at higher harmonics, some redox molecules would generate signals while others would not.
- FFT analysis all the various frequency components of a response to a sinusoidal input can be observed at once.
- JTFT joint time-frequency transform
- digital lock-in techniques are used.
- digitized raw data from the electrochemical cell have been analyzed by either fast Fourier transform or some complex form of joint time-frequency transform analysis.
- the major draw back of these methods is the enormous computational time associated with frequency transformation techniques.
- Digital lock-in is simple and fast.
- digital lock-in is identical to analog lock-in.
- the bandwidth narrowing process is done mathematically by multiplying the cell response by a sinusoidal with the same frequency as the input voltage, but with 90° phase shift.
- the technique has the same limitation as its analog counterpart since only one frequency can be analyzed at a time.
- other frequencies can also be analyzed sequentially (or in parallel with a more powerful processor) since the raw data is archived.
- background subtraction of the current vector and phase optimization is done.
- correlation and/or convolution techniques are used.
- signal recovery is done using signal recognition and background subtraction.
- the idea is to fit the cell response to two summed functions, one that describes the signal and the other that models the background capacitive current. Once the functions are constructed, the signal is easily recovered from the response by subtracting the fitted background capacitive current.
- This signal recognition scheme is applicable to any system where the signal has a behavior and shape that is relatively well known. The following example illustrates how such a scheme can be applied to the systems of the invention.
- the response from an electrochemical cell can be processed with a lock-in amplifier or equivalent bandwidth-narrowing technique. This is one of many methods of increasing signal to background using some form of bandwidth-narrowing technique.
- spectral analysis of the signal is done.
- filtering techniques in the frequency domain make use of means, variances, densities, autocorrelation functions, and power spectral densities of the signal and apply it to the present systems to enhance the signal to noise ratio (see Schwartz et al., Signal Processing: Discrete Spectral Analysis, Detection, and Estimation, N.Y. McGraw Hill, 1975, hereby incorporated by reference).
- digital filtering techniques are used. These include, but are not limited to, match filter, Weiner filtering, Kalman, Finite Impulse Response, infinite impulse response, narrow band filtering, etc.
- a match filter is used; see Ziemer et al., "Principles of Communication Systems, Modulation and Noise", 4th Ed. John Wiley & Sons Inc., New York, 465-471, 1988; and Helstrom, C. W., "Statistical Theory of Signal Detection", Pergamon Press, Oxford, 112-115, 1968, both of which are incorporated by reference.
- a match filter is a signal processing technique that "weights" the measured response (signal plus noise) samples by some corresponding known signal amplitude and convolutes the two signals to enhance signal to noise.
- a Weiner filter is used (see Press, supra; and Elliot et al., Fast Transforms: Algorithm, Analysis, Applications N.Y. Academic Press (1982), both of which are incorporated by reference).
- S( ⁇ ) R( ⁇ )£/( ⁇ )
- S, R, and U are the Fourier transform of s, r, and u, respectively.
- the uncorrupted signal can be recovered by finding the optimal filter ⁇ (t) or its Fourier counterpart ⁇ ( ⁇ ) which when applied to the measured signal c(t) or C( ⁇ ), and then deconvolved by r(t) or R( ⁇ ), produces a signal that approximates the uncorrupted signal u(t) or U( ⁇ ) with
- a kalman filter is used, which is a recursive-estimation filtering technique that tracks the current value of a changing signal in the presence of noise. See Kalman et al., A New Approach to Linear Filtering and Prediction Problems, Trans. ASME J. Basic Engineering, Seires D, 82, March 35, 1960; Elliot Ed. Handbook of Digital Signal Processing: Engineering Applications” , Academic Press, San Diego, p908, 1987; Chui et al., Kalman Filtering: with Real Time Applications", Springer-Verlag, New York, 1987; all of which are expressly incorporated by reference.
- the non-linear harmonic response is increased by inducing an asymmetrical response.
- this is done by using a system that has a non- reversible redox couple.
- ferrocene is a redox couple that is very reversible.
- the ferrocenes subtended by the ac voltage at a given point get oxidized on the upswing of the ac voltage and reduced on the down swing.
- a semi-reversible or non-reversible redox couple is used, for example, the molecule will get oxidized on the up swing and not reduced (or a portion) on the downswing; or vice versa. This will produce even greater non-linearities at certain frequencies.
- electron transfer is initiated using alternating current (AC) methods.
- AC alternating current
- the use of AC techniques allows the significant reduction of background signals at any single frequency due to entities other than the ETMs, i.e. "locking out” or “filtering” unwanted signals. That is, the frequency response of a charge carrier or redox active molecule in solution will be limited by its diffusion coefficient and charge transfer coefficient. Accordingly, at high frequencies, a charge carrier may not diffuse rapidly enough to transfer its charge to the electrode, and/or the charge transfer kinetics may not be fast enough. This is particularly significant in embodiments that do not have good monolayers, i.e. have partial or insufficient monolayers, i.e. where the solvent is accessible to the electrode.
- the presence of "holes" where the electrode is accessible to the solvent can result in solvent charge carriers “short circuiting" the system, i.e. they reach the electrode and generate background signal.
- one or more frequencies can be chosen that prevent a frequency response of one or more charge carriers in solution, whether or not a monolayer is present. This is particularly significant since many biological fluids such as blood contain significant amounts of redox active molecules which can interfere with amperometric detection methods.
- measurements of the system are taken at at least two separate frequencies, with measurements at a plurality of frequencies being preferred.
- a plurality of frequencies includes a scan. For example, measuring the output signal, e.g., the AC current, at a low input frequency such as 1 - 20 Hz, and comparing the response to the output signal at high frequency such as 10 - 100 kHz will show a frequency response difference between the presence and absence of the ETM.
- the frequency response is determined at at least two, preferably at least about five, and more preferably at least about ten frequencies.
- an output signal is received or detected.
- the presence and magnitude of the output signal will depend on a number of factors, including the overpotential/amplitude of the input signal; the frequency of the input AC signal; the composition of the intervening medium; the DC offset; the environment of the system; the nature of the ETM; the solvent; and the type and concentration of salt.
- the presence and magnitude of the output signal will depend in general on the presence or absence of the ETM, the placement and distance of the ETM from the surface of the monolayer and the character of the input signal. In some embodiments, it may be possible to distinguish between non-specific binding of label probes and the formation of target specific assay complexes containing label probes, on the basis of impedance.
- the output signal comprises an AC current.
- the magnitude of the output current will depend on a number of parameters. By varying these parameters, the system may be optimized in a number of ways.
- AC currents generated in the present invention range from about 1 femptoamp to about 1 milliamp, with currents from about 50 femptoamps to about 100 microamps being preferred, and from about 1 picoamp to about 1 microamp being especially preferred.
- the output signal is phase shifted in the AC component relative to the input signal.
- the systems of the present invention may be sufficiently uniform to allow phase-shifting based detection. That is, the complex biomolecules of the invention through which electron transfer occurs react to the AC input in a homogeneous manner, similar to standard electronic components, such that a phase shift can be determined. This may serve as the basis of detection between the presence and absence of the ETM, and/or differences between the presence of target-specific assay complexes comprising label probes and non-specific binding of the label probes to the system components.
- the output signal is characteristic of the presence of the ETM; that is, the output signal is characteristic of the presence of the target-specific assay complex comprising label probes and ETMs.
- the basis of the detection is a difference in the faradaic impedance of the system as a result of the formation of the assay complex.
- Faradaic impedance is the impedance of the system between the electrode and the ETM. Faradaic impedance is quite different from the bulk or dielectric impedance, which is the impedance of the bulk solution between the electrodes. Many factors may change the faradaic impedance which may not effect the bulk impedance, and vice versa.
- the assay complexes comprising the nucleic acids in this system have a certain faradaic impedance, that will depend on the distance between the ETM and the electrode, their electronic properties, and the composition of the intervening medium, among other things.
- the faradaic impedance between the ETM and the electrode is signficantly different depending on whether the label probes containing the ETMs are specifically or non-specifically bound to the electrode.
- the present invention further provides electronic devices or apparatus for the detection of analytes using the compositions of the invention.
- the apparatus includes a test chamber for receiving a sample solution which has at least a first measuring or sample electrode, and a second measuring or counter electrode. Three electrode systems are also useful.
- the first and second measuring electrodes are in contact with a test sample receiving region, such that in the presence of a liquid test sample, the two electrophoresis electrodes may be in electrical contact.
- the apparatus also includes detection electrodes comprising a single stranded nucleic acid capture probe covalently attached via an attachment linker, and a monolayer comprising conductive oligomers, such as are described herein.
- the apparatus further comprises an AC voltage source electrically connected to the test chamber; that is, to the measuring electrodes.
- the AC voltage source is capable of delivering DC offset voltage as well.
- the apparatus further comprises a processor capable of comparing the input signal and the output signal.
- the processor is coupled to the electrodes and configured to receive an output signal, and thus detect the presence of the target nucleic acid.
- the multiplexing devices and cartridges of the invention find use in a wide variety of applications.
- the compositions of the invention find use in hybridization assays.
- electrodes can be made that have a single species of nucleic acid, i.e. a single nucleic acid sequence, or multiple nucleic acid species.
- STRs short tandem repeats
- SNPs single nucleotide polymorphisms
- SNPs are likely to be the direct cause of therapeutically relevant phenotypic variants and/or disease predisposition.
- phenotypic variants and/or disease predisposition There are a number of well known polymorphisms that cause clinically important phenotypes; for example, the apoE2/3/4 variants are associated with different relative risk of Alzheimer's and other diseases (see Cordor et al., Science 261(1993)).
- Multiplex PCR amplification of SNP loci with subsequent hybridization to oligonucleotide arrays has been shown to be an accurate and reliable method of simultaneously genotyping at least hundreds of SNPs
- the present invention is directed to methods of determining the sequence of a target nucleic acid at a particular position, using electrochemical detection on an electrode.
- the invention preferably includes the detection (and optionally quantification) of differences or variations of sequences (e.g. SNPs) using electrode arrays for detection of the variation.
- compositions of the present invention may be used in a variety of research, clinical, quality control, or field testing settings.
- the probes are used in genetic diagnosis.
- probes can be made using the techniques disclosed herein to detect target sequences such as the gene for nonpolyposis colon cancer, the BRCA1 breast cancer gene, P53, which is a gene associated with a variety of cancers, the Apo E4 gene that indicates a greater risk of Alzheimer's disease, allowing for easy presymptomatic screening of patients, mutations in the cystic fibrosis gene, or any of the others well known in the art.
- viral and bacterial detection is done using the complexes of the invention.
- probes are designed to detect target sequences from a variety of bacteria and viruses. For example, current blood-screening techniques rely on the detection of anti- HIV antibodies.
- the methods disclosed herein allow for direct screening of clinical samples to detect HIV nucleic acid sequences, particularly highly conserved HIV sequences. In addition, this allows direct monitoring of circulating virus within a patient as an improved method of assessing the efficacy of anti-viral therapies. Similarly, viruses associated with leukemia, HTLV-I and HTLV-II, may be detected in this way. Bacterial infections such as tuberculosis, clymidia and other sexually transmitted diseases, may also be detected, for example using ribosomal RNA (rRNA) as the target sequences.
- rRNA ribosomal RNA
- the nucleic acids of the invention find use as probes for toxic bacteria in the screening of water and food samples.
- samples may be treated to lyse the bacteria to release its nucleic acid (particularly rRNA), and then probes designed to recognize bacterial strains, including, but not limited to, such pathogenic strains as, Salmonella, Campylobacter, Vibrio cholerae, Leishmania, enterotoxic strains of E. coli, and Legionnaire's disease bacteria.
- bioremediation strategies may be evaluated using the compositions of the invention.
- the probes are used for forensic "DNA fingerprinting" to match crime-scene DNA against samples taken from victims and suspects.
- the probes in an array are used for sequencing by hybridization.
- the present invention provides for extremely specific and sensitive probes, which may, in some embodiments, detect target sequences without removal of unhybridized probe. This will be useful in the generation of automated gene probe assays.
- compositions of the invention are useful to detect successful gene amplification in PCR, thus allowing successful PCR reactions to be an indication of the presence or absence of a target sequence.
- PCR may be used in this manner in several ways.
- the PCR reaction is done as is known in the art, and then added to a composition of the invention comprising the target nucleic acid with a ETM, covalently attached to an electrode via a conductive oligomer with subsequent detection of the target sequence.
- PCR is done using nucleotides labelled with a ETM, either in the presence of, or with subsequent addition to, an electrode with a conductive oligomer and a target nucleic acid.
- the nucleic acid attached to the electrode via a conductive polymer may be one PCR primer, with addition of a second primer labelled with an ETM. Elongation results in double stranded nucleic acid with a ETM and electrode covalently attached. In this way, the present invention is used for PCR detection of target sequences.
- the arrays are used for mRNA detection.
- a preferred embodiment utilizes either capture probes or capture extender probes that hybridize close to the 3' polyadenylation tail of the mRNAs. This allows the use of one species of target binding probe for detection, i.e. the probe contains a poly-T portion that will bind to the poly-A tail of the mRNA target. Generally, the probe will contain a second portion, preferably non-poly-T, that will bind to the detection probe (or other probe). This allows one target-binding probe to be made, and thus decreases the amount of different probe synthesis that is done.
- the use of restriction enzymes and ligation methods allows the creation of "universal" arrays.
- monolayers comprising capture probes that comprise restriction endonuclease ends as is generally depicted in Figure 7 of PCT US97/20014 .
- an array comprising any number of restriction endonuclease sites is made.
- Treating a target sample with one or more of these restriction endonucleases allows the targets to bind to the array. This can be done without knowing the sequence of the target.
- the target sequences can be ligated, as desired, using standard methods such as ligases, and the target sequence detected, using either standard labels or the methods of the invention.
- the present invention provides methods which can result in sensitive detection of nucleic acids.
- less than about 10 X 10 6 molecules are detected, with less than about 10 X 10 5 being preferred, less than 10 X 10 4 being particularly preferred, less than about 10 X 10 3 being especially preferred, and less than about 10 X 10 2 being most preferred.
- this assumes a 1:1 correlation between target sequences and reporter molecules; if more than one reporter molecule (i.e. electron transfer moeity) is used for each target sequence, the sensitivity will go up.
- the present invention utilizes electrochemical techniques to detect various biological and chemical targets.
- these techniques yield signals with an informative or a characteristic shape, size, and location.
- model It's generally possible to design a family of equations and a set of boundary conditions that describe the signals that can arise from a given measurement technique. This mathematical description is called a "model.” Sometimes the model is based on underlying scientific theory, but in many cases it may simply be an approximation that matches the observed signal behavior. In most cases the model is "non-linear,” comprising equations that are more complicated than basic polynomials.
- AC Alternating Current
- This technique yields an AC signal (a sine wave) that varies its amplitude (height, R) and phase (position, ⁇ ) as a function of the input DC voltage. As long as we monitor at a known frequency, it only takes two values to define such a wave.
- Figure 16 depicts a sine wave and its corresponding vector notation.
- the two values can be R and ⁇ , but as shown in the figure they can also be an (X,Y) pair separated by one quarter of an oscillation, i.e. by 90°.
- One way to simplify the visualization of such a system is by using what is called vector notation, demonstrated in four configurations in Figure 17.
- vector notation One important attribute of vector notation is that the vectors add exactly like the corresponding waves. For example, if two vectors point in roughly opposite directions, when they add they tend to cancel one another, leaving only a small residual vector. This exactly models how it is possible to add two waves together in such a way as to have "destructive interference," where the resulting amplitude is less than each of the inputs. As long as all waves have the same frequency, vectors will model their interference with one another.
- Figures 18 and 19 are examples of R and ⁇ traces for fourth harmonic AC voltammetry (AC voltage-4).
- the four-lobed shape in R-space is characteristic of medium to large signals, but as the signal shrinks relative to the size of the background, the R-space signal distorts. Furthermore, ⁇ traces of scans with larger signals are quite different from those with smaller ones. Figures 20 and 21 depict examples of a smaller signal.
- the smaller signal is now qualitatively similar to the medium signal, and is therefore more likely to be D described by the same mathematical model. Because of this, we chose to fit in X and Y. (For simplicity in conceiving a model and in computation during fitting, we chose to fit independently in X and Y instead of fitting both dimensions simultaneously.)
- V) I B (V) + ⁇ I S ⁇ n (V) n
- the Gaussian derivatives G x '" and G y '" each have three parameters: one for height, one for width, and one for location (in voltage).
- the height has no restrictions, corresponding only to the number of electrochemical labels that are signaling.
- a fit's width must fall within a reasonable range.
- signals in the independent X and Y fits must be close to one another (in voltage space) to assure that they both correspond to the same electrochemical label. Later I will discuss how these boundary conditions may be "enforced" to assure a meaningful fit.
- Instruments generally assign the X and Y axes based on the phase of the AC input driving force. ) Because this choice does not take into account the electrochemical system, it's possible that it may lead to the parallel/perpendicular trouble described above. Therefore, for signal recognition based on the above model, it's best to choose a new pair of axes assured to straddle any existing electrochemical signal.
- An advantage to this method is that the results are weighted by the length of the vectors of the original data points. That is, if a data point has a small amplitude (as it will if it represents a segment of a scan where no signal exists), it has a smaller impact on the value of the optimal phase. For example, if we add a small data point to the sample grouping, the results are shown in Figure 34 and 35. The new point changes the optimal phase by less than three degrees.
- the standard deviation of the data below the line is about 2V_ times larger than the standard deviation above.
- this rough method allows for the rapid detection and rejection of scans with large spikes.
- a ratio less than 2.25 and greater than 1/2.25 to be acceptable for further fitting.
- this value can depend on unusual parameter, such as scan length.
- the residual should be mostly signal (if any).
- the residual should be mostly signal (if any).
- the trace in Figure 55 has its largest value, 23.25, at a position of 0.20. The position matches well with the true data value. (Both are 0.20.)
- Figure 58 is the overlay of a real data trace and the corresponding initial guess.
- the initial guess is compared with the actual data, and the fit is altered based on this comparison in an attempt to minimize the "error".
- the data doesn't match the entire shape described by the model, it's possible that the alterations to the fit won't reduce the error. (This will happen, for example, if the scan contains neither a signal nor noise that looks like a signal.) If the error doesn't become smaller than the precision within the "maximum number of iterations" (also a pre-set constant), the fit is said to have "diverged”.
- the error and precision are often defined such that their values have units. For example, if the data is a current measured in picoamps, then the error and precision are in picoamps squared. This is most useful when all expected signals are of similar size, because it considers everything in absolute terms and will not attempt to optimize fits to small features.
- quantitative analytical techniques generally require a wide dynamic range. For example, one may need to examine signals that are two picoamps tall with the same ease as one examines two billion picoamp signals. To achieve such a dynamic range, we normalize data to the initial guess for the signal height. This allows the small signals to be fit just as well as the large, with only the shape and the background noise affecting the fit.
- boundary conditions arose earlier when discussing the choice of a model. For some systems, certain parameters may be reasonable only within a certain range. For example, for AC voltage-4 the width of the center two lobes of a sensor signal always falls between 110 and 265 mV, and is most commonly between 150 and 200 mV. There are several ways to enforce these boundaries, two of which are discussed here.
- N is the number of data points
- F is the value of the fit for data point number /
- D is the corresponding data value
- E R must be less than some empirically-determined value in order for the fit to be considered as having locked into a true signal.
- Figure 63 is the R composite
- * * X + Y is the R composite with the background polynomials subtracted
- the filtered residual can be quantified as follows:
- Non-linear regression techniques can reliably extract values from noisy data, but they are iterative processes, and as such can take large amounts of computational time.
- This example uses only sums (and differences), and then renormalization and a basic coordinate transformation. As such, it is extremely rapid. Also, the sums which comprise all of the data reduction (from some large number of points per cycle to just two points per cycle) can easily be programmed into an embedded device, thus allowing more rapid data transfer from the acquisition device (e.g. the instrument of the invention) to the data manipulation and storage device (e.g. computer).
- acquisition device e.g. the instrument of the invention
- data manipulation and storage device e.g. computer
- DNA hybridization assays on an eSensorTM chip typically require an incubation time of 4 to 6 hours for a 10 nM range target concentration. This time period was chosen based on diffusion based hybridization times in large volume (i.e., 0.5 ml) cartridges. However, for smaller volume cartridges (i.e., 100 ⁇ l), a 4 to 6 hour incubation time is not sufficient to achieve saturated hybridization signals. Thus, a number of different convective mixing techniques were evaluated in an eSensor TM chip in order to accelerate DNA hybridization.
- HFE-H was chosen as the model assay system. All chips and reagents used were from the same stock in order to eliminate sample or chip performance variations: Chips used: DC_668 Capture probe: D2002
- Hybridization buffer prepared according to standard protocols
- Heating systems Depending on the type of mixing used, different methods of heating were employed. For example, chips were incubated in a convective oven or on chip heating devices were used. Controls: Diffusion based hybridization was used as the control
- Chips were attached to a mini-peristaltic pump using micro bore peek tubing with a total dead volume of nearly 7 ⁇ l ( ⁇ 10% of chip volume of 8- to 100 ⁇ l). The fluid was recirculated at approximately 100 ⁇ l/min. The entire pump, tubing and chip assembly was placed inside an oven at 35°C. Measurements were made in real time by placing the eSensorTM-600board inside the oven. Saturation signals for the pumped chips were obtained within 1 hour. See Figure 70B.
- Bubble Assisted Piezo (PZT) Mixing Cartridge covers were drilled with 500 ⁇ m diameter holes that served as sites for bubbles when the hybridization buffer was added to the chip.
- a piezo-electric transducer was glued on the back of the cartridge and excited with 5 Khz a.c. waveform at 10Vp-p. This device was operated in two modes, a square wave or a sine wave excitation waveform.
- PZT based chips performed better than diffusion contols, requiring 2.5 hours to reach saturation. See Figure 70C.
- a thermal gradient was created across an assembled chip by heating the bottom of the chip to 65°C and cooling the top of the cartridge cover to 10°C.
- the thermal gradient was created by jacketing the chip between two peltier heaters.
- the diffusion control chip was heated using a peltier heater rather than the convective oven. Using peltier heating improved hybridization kinetics in the vertical diffusion control chip such that a saturation signal was observed within 2 hours.
- the chip in which thermal gradient mixing was used performed even better and reached saturation values within one hour. See Figure 70D.
- a microchannel was place on top of the eSensorTM chip by cutting adhesive tape into approximately 1 mm wide thin strips and placing these strips on top of the eSensorTM chip.
- a bubble was intentionally introduced into one corner of the chip. This bubble was then utilized to enhance mixing by alternately expanding and contracting the bubble volume by heating and cooling the bubble area. This approach allows mixing due to the pressure flow created by changing the volume of the bubble within the chip.
- the addition of microchannels decreased the chip volume to approximately 20 ⁇ l, resulting in slower kinetics in this system. Using the bubble pump accelerated the kinetics, but the kinetics were still not as good as observed with other mixing techniques. Typical results are shown in Figure 70E.
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Abstract
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US09/760,384 US7312087B2 (en) | 2000-01-11 | 2001-01-11 | Devices and methods for biochip multiplexing |
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PCT/US2001/044364 WO2002043864A2 (fr) | 2000-11-03 | 2001-11-05 | Dispositifs et procedes de multiplexage de puces a adn |
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- 2001-11-05 AU AU2002239354A patent/AU2002239354A1/en not_active Abandoned
- 2001-11-05 CA CA002427669A patent/CA2427669A1/fr not_active Abandoned
- 2001-11-05 JP JP2002545830A patent/JP2004515231A/ja active Pending
- 2001-11-05 EP EP01987105A patent/EP1331999A2/fr not_active Withdrawn
- 2001-11-05 WO PCT/US2001/044364 patent/WO2002043864A2/fr active Application Filing
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US9321053B2 (en) | 2012-08-30 | 2016-04-26 | Life Technologies Corporation | Vertical clamp device |
US9527084B2 (en) | 2012-08-30 | 2016-12-27 | Life Technologies Corporation | Vertical clamp device |
Also Published As
Publication number | Publication date |
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WO2002043864A2 (fr) | 2002-06-06 |
CA2427669A1 (fr) | 2002-06-06 |
JP2004515231A (ja) | 2004-05-27 |
AU2002239354A1 (en) | 2002-06-11 |
WO2002043864A3 (fr) | 2002-08-01 |
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